The Recall Desk

Archive

December 2013 recalls

1,402 recalls were announced in December 2013.

What the numbers show

Critical
351
Severe
605
High
191
Moderate
225
Low
30

Of the 1,402 recalls this month scored against our rubric, 25% are Critical, 43% are Severe.

401–500 of 1402

  • ModerateFDA (Food)·F-0797-2014·2013-12-25

    National Enzyme Recalls Bulk Enzyme Powder Due to Chloramphenicol Contamination

    National Enzyme Co is recalling bulk enzyme powder that may contain chloramphenicol above the permitted limit.

    Product
    Bulk C184 Ace Health Enzyme Blend powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83403);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0513-2014·2013-12-25

    Microgenics Recalls CEDIA Tobramycin II Assay Due to Calibration Stability Issues

    Microgenics Corp. is recalling CEDIA Tobramycin II Assay (Lot 60169764) due to a calibration stability problem identified through two customer complaints.

    Product
    Thermo Fisher Scientific/Microgenics brand CEDIA Tobramycin II Assay, Catalog Number 100018, Product is manufactured and distributed by Microgenics Corporation, located at Fremont, CA., part of Thermo Fisher Scientific The CEDIA Tobramycin II Assay is an in vitro diagnostic…
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·F-0844-2014·2013-12-25

    A&C US Trading LLC Recalls Lam Sheng Kee Haw Flakes for Unapproved Food Coloring

    A&C US Trading LLC is recalling Lam Sheng Kee Haw Flakes because the product contains unapproved food coloring. The recall affects 600 cartons distributed in New York.

    Product
    Lam Sheng Kee HAW FLAKES, NET WEIGHT 380 g (13.4 oz), product is packaged in plastic bag with twenty four (24) bags per carton. UPC 6 949682 803780. Manufactured by LAM SHENG KEE (HK) INTERNATIONAL LIMITED, RM3/8F., YUEXIU BLDG., 160-174 LOCKHART ROAD, WAN CHAI, HK.…
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0762-2014·2013-12-25

    National Enzyme Recalls Kirkman Bacterial Bio 6 Supplements for Chloramphenicol

    National Enzyme Co is recalling 9326 Kirkman Bacterial Bio 6 dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    9326 Kirkman Bacterial Bio 6, packaged in unlabeled 60-capsule bottles (SKU 53666);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0786-2014·2013-12-25

    National Enzyme Recalls Bulk Digestion Powder Due to Chloramphenicol

    National Enzyme Co is recalling Bulk B199 Reviva Digestion Bulk powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk B199 Reviva Digestion Bulk powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83342).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0759-2014·2013-12-25

    National Enzyme Co Recalls Dietary Supplements Due to Chloramphenicol Contamination

    National Enzyme Co is recalling specific dietary supplements because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configurations: (1) Natural Health Industries, Opti-Zyme HP, packaged in 90-capsule bottles (SKU 54654). Firm name on the label is Natural Health Industries, Clarmonte, CA; (2) 8974 Enzymes Inc Natural Hea, packaged in unlabeled…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0765-2014·2013-12-25

    National Enzyme Recalls BioSan Labs Capsules Due to Chloramphenicol

    National Enzyme Co is recalling BioSan Labs Hi Potency capsules because the raw material may contain chloramphenicol above 0.3 ppb.

    Product
    Bulk 9665 BioSan Labs Hi Potency capsules, packaged in poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92093);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0770-2014·2013-12-25

    National Enzyme Co Recalls Bulk Digest Platinum Capsules for Chloramphenicol

    National Enzyme Co is recalling bulk Digest Platinum capsules because they may contain chloramphenicol above 0.3 ppb.

    Product
    Bulk 9843 NOW Digest Platinum BLK capsules, packaged in poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92101).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0734-2014·2013-12-25

    National Enzyme Recalls TriEnza Supplements Due to Potential Chloramphenicol Contamination

    National Enzyme Co is recalling TriEnza digestive enzyme supplements because they may contain chloramphenicol above 0.3 ppb.

    Product
    Houston Enzymes TriEnza with DPP IV Activity, Broad-Spectrum Enzyme Product for general Digestive Support, packaged in 90-(SKU 53379) and 180-(SKU 53380) capsule bottles. The firm name on the label is Houston Nutraceuticals, Inc. (HNI), Siloam Springs, AR (2) 9212 TRIENZA Bulk…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0749-2014·2013-12-25

    National Enzyme Co Recalls Wellzymes Protein/Fat Digestion Enzyme Supplement

    National Enzyme Co is recalling Wellzymes enzyme supplements because a raw material may contain chloramphenicol above the 0.3 ppb limit.

    Product
    WELLZYMES, Protein/Fat Digestion, Enzyme Supplement packaged in 90-capsule bottles (SKU 52643). Manufactured exclusively for enzymes, inc., Kansas City, MO.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0773-2014·2013-12-25

    National Enzyme Co Recalls Dietary Supplements Due to Chloramphenicol

    National Enzyme Co is recalling NWC Naturals dietary supplements because a raw material may contain chloramphenicol above 0.3 ppb.

    Product
    NWC Naturals, Total-Nutrition Program, Dietary Supplement with L.E.A.D.S., packaged 270-capsule bottles (SKU 92131). Firm name on the label is Natural Wellness Centers of America, Inc., Laguna Hills, CA;
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0836-2014·2013-12-25

    Nature's Way Multivitamin Recalled for Potential Chloramphenicol Contamination

    Schwabe North America is voluntarily recalling Nature's Way Alive Once Daily MultiVitamin Ultra Potency tablets because raw material enzymes may contain the antibiotic chloramphenicol.

    Product
    Nature's Way,UPC 33674156797, Alive Once Daily MultiVitamin Ultra Potency, 60 Tabs, 20008123, 20010552
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Food)·F-0839-2014·2013-12-25

    Nature's Way Women's 50+ Probiotic Recalled for Potential Chloramphenicol Contamination

    Schwabe North America is voluntarily recalling Nature's Way Alive Once Daily Women's 50+ probiotic tablets because raw material enzymes may contain the antibiotic chloramphenicol.

    Product
    Nature's Way, UPC 33674156926, Alive Once Daily Women's 50+, 60 Tabs, 20007818, 20011423.
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Food)·F-0799-2014·2013-12-25

    National Enzyme Co Recalls Dietary Supplements Due to Chloramphenicol Contamination

    National Enzyme Co is recalling Heryben and Bulk C269 dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configurations: (1) Heryben, Eumin Integrated Plant Enzymes, packaged 60 capsule bottles(SKU 54440). Firm name on the label is ActiFit Biotechnology, Bellevue, WA; (2) Bulk C269 Shanghai Digestive Blen capsules, packaged in…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0507-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.

    Product
    Stryker brand COMPLIANT 4MM X 20MM, Catalog Number: M003SRC04200; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0776-2014·2013-12-25

    National Enzyme Recalls Dietary Supplements Due to Potential Chloramphenicol Contamination

    National Enzyme Co is recalling bulk dietary supplement capsules because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplement Formula ID A200; Packaged in the following configuration: Bulk A200 Nutr Provider Comp Dige capsules (SKU 92132), packaged in varying quantities within poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0526-2014·2013-12-25

    Karl Storz Recalls Flexible Intubation Fiberscopes Due to Material Issue

    Karl Storz Endoscopy America is recalling specific flexible intubation fiberscopes because the suction channel material is incompatible with STERRAD sterilization systems.

    Product
    Intubation Flexible Fiberscope, Models: 11301AA1, 11301BN1, 11302BD1, 11302BD2, 11304BC1, 11340BC1, 11301BND1, 11302BDD1, and 11302BDD2. " Transoral intubation " Transnasal intubation " Evaluation of placement of endotracheal and double lumen endotracheal tubes " Provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0798-2014·2013-12-25

    National Enzyme Recalls Multi Plant Enzyme Tablets Due to Chloramphenicol

    National Enzyme Co is recalling Multi Plant Enzyme Tablets because a raw material may contain chloramphenicol above 0.3 ppb.

    Product
    Multi Plant Enzyme Tablets, packaged 60 tablet bottles(SKU 54451). Firm name on the label is Wedar Nutrasource Inc., Hacienda Height, CA;
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0813-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive Powder Due to Chloramphenicol

    National Enzyme Co is recalling bulk D103 Life Tree Digestive Ble powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk D103 Life Tree Digestive Ble powder packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83466).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0777-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive Supplement Capsules Due to Chloramphenicol

    National Enzyme Co is recalling bulk digestive supplement capsules because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk A213 Phion Complete Digestiv capsules (SKU 92123), packaged in varying quantities within poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0739-2014·2013-12-25

    National Enzyme Co Recalls Digest Enzyme Supplements Due to Chloramphenicol

    National Enzyme Co is recalling various digest enzyme supplements because they may contain chloramphenicol above 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configurations: (1)Transformation Professional Protocol Digest Enzyme Supplement, Packaged in 45-(SKU 54646), 60-(SKU 52413), 90-(SKU 52520), 120-(SKU 53098) capsule bottles. The firm name on the label is Transformation Enzyme…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0519-2014·2013-12-25

    Beckman Coulter Recalls Access Immunoassay Reaction Vessels Due to Motion Errors

    Beckman Coulter is recalling Access Immunoassay Reaction Vessels due to intermittent wash carousel motion errors affecting specific lots.

    Product
    Access Immunoassay Systems Reaction Vessels. The Access Immunoassay System is an in vitro diagnostic device used for the quantitative, semi-quantitative or qualitative determination of various analyte concentrations found in human body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0504-2014·2013-12-25

    Stryker Neurovascular Medical Devices Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates exceeding available shelf-life data.

    Product
    Stryker brand GDC VORTX 2MM X 3MM, Catalog Number: M00335302340; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-366-2014·2013-12-25

    Airgas Recalls Carbon Dioxide Cylinders Due to Labeling Error

    Airgas Medical Services is recalling 264 carbon dioxide cylinders because one was incorrectly labeled as a gas withdrawal cylinder instead of a liquid withdrawal cylinder.

    Product
    Carbon Dioxide, USP, Medical Gas, Rx only, Non Flammable Gas 2, in 50 lbs steel cylinders, Distributed by AIRGAS USA, LLC Radnor, PA
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Food)·F-0789-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive Supplement Due to Chloramphenicol

    National Enzyme Co is recalling bulk B807 True Botanica Digestive dietary supplements because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk B807 True Botanica Digestive, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83377);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-351-2014·2013-12-25

    Tween Brands Recalls Hand Sanitizer with Incorrect Alcohol Labeling

    Tween Brands is recalling 42,570 units of Green Apple hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.

    Product
    Girls can change the World, Green Apple Anti bac Justice, Ethyl Alcohol, Net Wt 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5 Made in China
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0512-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates that exceed available shelf-life data.

    Product
    Stryker brand SUPER COMPLIANT 7MM X 15MM, Catalog Number: M003SSC07150; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0535-2014·2013-12-25

    3M ESPE Imprint II and Paradigm Impression Materials Recalled for Quality Issues

    3M is recalling specific lots of Imprint II and Paradigm dental impression materials because a defect reduces moisture displacement, potentially affecting impression quality.

    Product
    3M ESPE Imprint II Regular Body , Catalog Number 9379, and Paradigm Regular Body VPS, Catalog Number 5315, Impression Material that are intended to reproduce the structure of a patients teeth. Impression Materials are composed of hydrophilic vinyl polysiloxane impression…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0527-2014·2013-12-25

    Karl Storz Recalls Flexible Broncho Fiberscopes Due to Material Issue

    Karl Storz Endoscopy America is recalling 141 flexible broncho fiberscopes because the suction channel material is not listed for STERRAD sterilization systems.

    Product
    Broncho Flexible Fiberscope, models: 11001BN1, 11002BD1, 11004BC1, and 11009BC1. " Examination and treatment of the tracheobronchial tree Contraindications for Bronchoscopy " Uncontrolled angina, uncontrolled heart failure, or serious uncontrolled ventricular arrhythmias "…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0831-2014·2013-12-25

    Nature's Way Recalls Alive Whole Food Energizer with Iron Due to Antibiotic Risk

    Schwabe North America is voluntarily recalling Nature's Way Alive Whole Food Energizer with Iron because raw material enzymes may contain the antibiotic chloramphenicol.

    Product
    Nature's Way, UPC 33674149263, Alive Whole Food Energizer with Iron, 60 Tabs 20009807; Nature's Way, UPC 33674149270, Alive Whole Food Energizer with Iron, 90 Tabs 20009808. 33674149287 Alive Whole Food Energizer with Iron, 180 Tabs 20012063
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Food)·F-0838-2014·2013-12-25

    Nature's Way Recalls Women's Multivitamin Due to Potential Antibiotic Contamination

    Schwabe North America is voluntarily recalling Nature's Way Alive Once Daily Women's Ultra Potency tablets because the raw material supplier reported that enzymes in the blend may contain the antibiotic chloramphenicol.

    Product
    Nature's Way,UPC 33674156865, Alive Once Daily Women's Ultra Potency, 60 Tabs, 20010554, 20011595, 20014135
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Food)·F-0756-2014·2013-12-25

    National Enzyme Recalls GreenPlanet Enzymeblend Powder Due to Chloramphenicol

    National Enzyme Co is recalling GreenPlanet Enzymeblend Powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk 7775 GreenPlanet Enzymeblend Powder packaged in poly bags within fiber drums (SKU 82566)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0500-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling specific microcatheter and coil products because they were shipped with use-by dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED 90 150CM, Catalog Number: M0031681910; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0801-2014·2013-12-25

    National Enzyme Recalls Travnie Extra Due to Potential Chloramphenicol Contamination

    National Enzyme Co is recalling Travnie Extra dietary supplements because they may contain chloramphenicol above 0.3 ppb.

    Product
    Enzyme - Travnie Extra, Formula C500, packaged in 30-capsule bottles (SKU 54513). Firm name on the label is National Enzyme Company;
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0515-2014·2013-12-25

    Instrumentation Laboratory Recalls HemosIL Low Abnormal Control 2 Kits

    Instrumentation Laboratory is recalling 6,504 kits of HemosIL Low Abnormal Control 2 UNASSAYED because the product lacks FDA 510(k) approval.

    Product
    HemosIL Low Abnormal Control 2 UNASSAYED Part Number: 0020003220
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1109-2014·2013-12-25

    LSG Food World Recalls Noodles House Home Style Noodles for Unapproved Additives

    LSG Food World Inc. is recalling Noodles House Home Style Noodles because the product contains an unapproved color and an undeclared food additive.

    Product
    NOODLES HOUSE HOME STYLE NOODLES, Net Wt. 900 g (31.7 oz), product is packaged in plastic bag with twelve (12) bags per carton. UPC 6 949682 801755; Manufactured by: S&M(HK) ENTERPRISE LTD. RM3.8/F., YUEXIU BLDG., 160-174 LOCKHART ROAD, WAN CHAI, HK. Distributed by: S&M INT'L…
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-349-2014·2013-12-25

    Tween Brands Recalls Share a Smile Hand Sanitizer Due to Label Error

    Tween Brands Inc is recalling Share a Smile Mixed Berry hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.

    Product
    Share a Smile Mixed berry Anti bac Justice, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0497-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling Excelsior SL-10 microcatheters because they were shipped with use-by dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED S 15OCM; Catalog Number: M0031441920; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0783-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive Blend Powder Due to Chloramphenicol

    National Enzyme Co is recalling bulk A977 Wedar Digestive Blend 2 powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk A977 Wedar Digestive Blend 2 powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83314);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0802-2014·2013-12-25

    National Enzyme Recalls Bulk Vitakost Low Carb Diet Due to Chloramphenicol

    National Enzyme Co is recalling Bulk C542 Vitakost Low Carb Diet because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk C542 Vitakost Low Carb Diet, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92544);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0543-2014·2013-12-25

    CooperVision Recalls ClearSight Toric Contact Lenses for Incorrect Expiration Dates

    CooperVision is recalling specific lots of ClearSight Toric 1 day contact lenses because the outer cartons display incorrect expiration dates, though the inner blisters are correct.

    Product
    ClearSight(TM) Toric 1 day (ocufilcon D), 30 daily disposable contact lenses for astigmatism, STERILE, Rx only --- CooperVision Hamble, SO31 4RF, UK - Scottsville, NY 14546 USA - Juana Diaz, PR 00795 USA daily use disposable contact lenses for astigmatism
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0796-2014·2013-12-25

    National Enzyme Recalls BioSan Enzyme Blend Capsules Due to Chloramphenicol

    National Enzyme Co is recalling BioSan Enzyme Blend 3 O capsules because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk C012 BioSan Enzyme Blend 3 O capsules,packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92438);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0499-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Shelf-Life Labeling Errors

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED 45 150CM, Catalog Number: M0031681900, Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0809-2014·2013-12-25

    National Enzyme Recalls ZoiVi Digestive Formula Powder Due to Chloramphenicol

    National Enzyme Co is recalling ZoiVi Digestive Formula powder because it may contain chloramphenicol above 0.3 ppb.

    Product
    Bulk C812 ZoiVi Digestive Formula powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83438)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0755-2014·2013-12-25

    National Enzyme Recalls Dietary Supplements Due to Potential Chloramphenicol Contamination

    National Enzyme Co is recalling specific dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configurations: (1) 7263 Kirk Enz-Comp-W-TG UNL, packaged in unlabeled, 90-capsule bottles (SKU 52939); (2) 7263 Kirk Enz-Comp-W-TG UNL2, packaged in unlabeled 180-capsule bottles (SKU 53852);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0492-2014·2013-12-25

    Aesculap Columbus Revision CoCr Spacers Recalled Due to Incompatibility

    Aesculap, Inc. is recalling 24 Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7, because they were not compatible.

    Product
    Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Food)·F-1112-2014·2013-12-25

    OneBode Flo Probiotic Supplements Recalled for Chloramphenicol Contamination

    Global Health Laboratories is recalling OneBode Flo probiotic supplements found to contain chloramphenicol, an antibiotic, above permitted levels.

    Product
    (a) ONEBODE Flo daily, probiotic enzyme digestive, 90 capsules, dietary supplement, Product No. T00135, UPC 0 14834 00135 5; (b) ONEBODE Flo for Family, probiotic enzyme digestive, 360 capsules, dietary supplement, Product No. T00109, UPC 0 14834 00109 6; (c) ONEBODE Flo daily…
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0805-2014·2013-12-25

    National Enzyme Recalls Colon Health Support Due to Chloramphenicol

    National Enzyme Co is recalling Healthy Reflections Colon Health Support supplements because a raw material may contain chloramphenicol above 0.3 ppb.

    Product
    Healthy Reflections, Colon Health Support, packaged 120-capsule bottles (SKU 54554). Firm name on the label is Healthy Reflections, Garfield, MN;
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0495-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Shelf-Life Labeling Errors

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates that exceed available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM; Catalog Number: M0031441930; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0779-2014·2013-12-25

    National Enzyme Recalls Bulk Enzyme Powder for Potential Chloramphenicol

    National Enzyme Co is recalling bulk enzyme powder that may contain chloramphenicol above 0.3 ppb.

    Product
    Bulk A322 Houston Chewable Enzyme powder (SKU 83226), packaged in varying quantities within poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0832-2014·2013-12-25

    Nature's Way Recalls Alive Whole Food Energizer Due to Antibiotic Concerns

    Schwabe North America is voluntarily recalling Nature's Way Alive Whole Food Energizer tablets because raw material enzymes may contain the antibiotic chloramphenicol.

    Product
    Nature's Way,UPC 33674149324 Alive Whole Food Energizer ,180 Tabs, 20009819, 20012443
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Food)·F-0741-2014·2013-12-25

    National Enzyme Co Recalls Wellzymes Digestive Health Enzyme Supplement

    National Enzyme Co is recalling Wellzymes Digestive Health Enzyme Supplement bottles because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    WELLZYMES, Digestive Health, Enzyme Supplement packaged in 60-(SKU 52235) capsule bottles. Manufactured exclusively for enzymes, inc. Kansas City, MO
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0501-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling certain microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM, Catalog Number: M0031681920; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0735-2014·2013-12-25

    National Enzyme Co Recalls Dietary Supplements for Potential Chloramphenicol Contamination

    National Enzyme Co is recalling specific dietary supplement bottles because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplement packaged in the following configuration: (1)Nutri-Essence Digestion Super Potency Enzymes & Herbs with patent-pending CereCalase Plus, packaged in 180-(SKU 51832) capsule bottles. The firm name on the label is Enzymes, Inc., Parkville, MO (2) Positive…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0793-2014·2013-12-25

    National Enzyme Recalls Vitamin Shoppe Advanced Powder Due to Chloramphenicol

    National Enzyme Co is recalling Bulk B983 Vitamin Shoppe Advanced powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk B983 Vitamin Shoppe Advnaced powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83408);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0740-2014·2013-12-25

    National Enzyme Recalls OxiCellZyme Supplements Due to Chloramphenicol Contamination

    National Enzyme Co is recalling OxiCellZyme enzyme supplements because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    enzyme essentials, OxiCellZyme, Enzyme Supplement with Herbs, packaged in 90-(SKU 54929) and 180-(SKU 52270) capsule bottles.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0784-2014·2013-12-25

    National Enzyme Recalls Digestive Enzyme Supplements Due to Chloramphenicol

    National Enzyme Co is recalling 1,751 bottles of Healthy Digest dietary supplements because they may contain chloramphenicol above 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configuration: (1) Competitive Nutrition, Healthy Digest, packaged in 90-capsule bottles (SKU 83314). Firm name on the label is Competitive Nutrition, Monaca, PA; (2) New Earthlings Nutritionals, Healthy Digest, Complete Digestive…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0791-2014·2013-12-25

    National Enzyme Recalls Bulk TriEnz Powder Due to Chloramphenicol

    National Enzyme Co is recalling bulk TriEnz powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk B910 Houston Nutr TriEnz Bu powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83381);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0769-2014·2013-12-25

    National Enzyme Recalls DigestBasicK Capsules Due to Chloramphenicol Contamination

    National Enzyme Co is recalling specific lots of DigestBasicK capsules because they may contain chloramphenicol above 0.3 ppb.

    Product
    Bulk 9835 ENZYMEDICA DIGESTBASICK capsules, packaged in poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92085).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1114-2014·2013-12-25

    DRUK Mango Squash Recalled for Undeclared Artificial Dyes

    Balajee Trade Link LLC is recalling DRUK Mango Squash because FDA testing found undeclared artificial dyes, tartrazine and sunset yellow FCF.

    Product
    DRUK Mango Squash Contains 25% Mango Pulp Net Wt. 24 fl oz. Imported by: Balajee Trade Link, LLC Scranton, PA USA Product of Bhutan
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-0811-2014·2013-12-25

    National Enzyme Recalls Digestion Support Supplements Due to Chloramphenicol

    National Enzyme Co is recalling Healthy Alternatives Digestion & Stomach Upset Support supplements because they may contain chloramphenicol above 0.3 ppb.

    Product
    Healthy Alternatives, Digestion & Stomach Upset Support, packaged 90-capsule bottles (SKU 54897). Firm name on the label is Health Enhancement, Inc. Grass Valley, CA;
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0747-2014·2013-12-25

    National Enzyme Recalls Kirkman Enzym-Complete Supplements Due to Chloramphenicol

    National Enzyme Co is recalling specific lots of Kirkman Enzym-Complete dietary supplements because they may contain chloramphenicol above 0.3 ppb.

    Product
    Dietary Supplement packaged in the following configurations: (1) KIRKMAN, Enzym-Complete / DPP-IV, Broad Spectrum Digestion Formula with Dipeptidyl Peptidase IV Analog, packaged in 60-capsule bottles (SKU 52587), 120-capsule bottles (SKU 52588), and 200-capsule bottles (SKU…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0508-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.

    Product
    Stryker brand COMPLIANT 4MM X 30MM, Catalog Number: M003SRC04300; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0806-2014·2013-12-25

    National Enzyme Co Recalls Dietary Supplements Due to Chloramphenicol Contamination

    National Enzyme Co is recalling specific dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configurations: (1) No-Fenol Chewable, Multi-Enzyme Product for Digestion of Phenolic Foods and Fibers, packaged 180-chewable tablets bottles (SKU 54651). Firm name on the label is Houston Nutraceutical Inc. (HNI), Siloam, AR; (2)…
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-363-2014·2013-12-25

    Tween Brands Recalls Grape Scented Anti-Bac Due to Labeling Error

    Tween Brands Inc is recalling 15,931 bottles of Grape Scented Anti-Bac because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.

    Product
    YOU CANT HANDLE THIS Justice, GRAPE SCENT ANTI BAC, Ethyl Alcohol Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-356-2014·2013-12-25

    Tween Brands Recalls Grape Anti-Bac Hand Sanitizer Due to Label Error

    Tween Brands Inc is recalling 21,201 bottles of I love sleep overs Justice, Grape anti bac hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.

    Product
    I love sleep overs Justice, Grape anti bac, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-357-2014·2013-12-25

    Tween Brands Recalls Peach Anti-Bac Hand Sanitizer Due to Label Error

    Tween Brands Inc is recalling 23,231 bottles of Peach anti-bac hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.

    Product
    I love to shop Justice, Peach anti bac, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-362-2014·2013-12-25

    Tween Brands Recalls I Love Bacon Justice Hand Sanitizer Due to Label Error

    Tween Brands Inc is recalling 16,471 bottles of I Love Bacon Justice hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.

    Product
    I LOVE BACON Justice, VANILLA scent anti bac, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-379-2014·2013-12-25

    Fresenius Kabi Recalls Folic Acid Injection Vials for Impurity Failures

    Fresenius Kabi USA is recalling folic acid injection vials due to failed impurity and degradation specifications at 14 and 15 months.

    Product
    FOLIC ACID INJECTION, USP; 5 mg/mL ; For IM, IV or SC Use; 10 mL; Multiple Dose Vial; Rx only; APP Pharmaceuticals, LLC; Schaumburg, IL 60173 NDC 63323-184-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-365-2014·2013-12-25

    Tween Brands Recalls Cherry Scent Anti Bac Due to Label Error

    Tween Brands Inc is recalling 4,692 bottles of BFF's are COOL! Justice Cherry Scent Anti Bac because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.

    Product
    BFF's are COOL! Justice, CHERRY SCENT ANTI BAC, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-361-2014·2013-12-25

    Tween Brands Recalls Cotton Candy Scented Hand Sanitizer Due to Labeling Error

    Tween Brands Inc is recalling 20,167 bottles of 'I MUSTACHE YOU TO BE MY BFF' hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.

    Product
    I MUSTACHE YOU TO BE MY BFF Justice, COTTON CANDY scent anti bac, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-358-2014·2013-12-25

    Tween Brands Recalls Lemon Anti Bac Justice Due to Label Error

    Tween Brands Inc is recalling 27,590 bottles of Lemon Anti Bac Justice because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.

    Product
    Lemon anti bac Justice, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-354-2014·2013-12-25

    Tween Brands Recalls Anti-Bacterial Hand Sanitizer Due to Labeling Error

    Tween Brands Inc is recalling 58,054 bottles of LIFE IS SWEET! Justice hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.

    Product
    LIFE IS SWEET! Justice, Vanilla Scent anti bac, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-348-2014·2013-12-25

    Tween Brands Recalls Strawberry Hand Sanitizer Due to Labeling Error

    Tween Brands Inc is recalling 86,701 bottles of Believe in Yourself Strawberry Anti bac Justice hand sanitizer because the label incorrectly states the ethyl alcohol content.

    Product
    Believe in Yourself Strawberry Anti bac Justice, Ethyl Alcohol, Net Wt 1 fl oz., Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-359-2014·2013-12-25

    Tween Brands Recalls Grapefruit Anti Bac Justice Due to Label Error

    Tween Brands Inc is recalling 18,492 bottles of Grapefruit anti bac Justice because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.

    Product
    Grapefruit anti bac Justice, Ethyl Alcohol, Net Wt. 1 fl oz, Tocopheryl Acetate,*** Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-355-2014·2013-12-25

    Tween Brands Recalls Watermelon Hand Sanitizer Due to Label Error

    Tween Brands Inc is recalling 47,051 bottles of 'I love my BFF Justice' Watermelon anti-bac hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% when it is actually 20%.

    Product
    I love my BFF Justice, Watermelon anti bac, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-360-2014·2013-12-25

    Tween Brands Recalls Girls Rock Justice Hand Sanitizer Due to Label Error

    Tween Brands Inc is recalling 9,558 bottles of Girls Rock Justice hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.

    Product
    GIRLS ROCK Justice, VANILLA scent anti bac, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-352-2014·2013-12-25

    Tween Brands Recalls Justice Anti-Bacterial Hand Sanitizer Due to Labeling Error

    Tween Brands Inc is recalling 65,332 bottles of Justice Chocolate anti-bacterial hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.

    Product
    FOLLOW YOUR DREAMS! Justice, Chocolate anti bac, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0528-2014·2013-12-25

    Remel Recalls Oxoid Ciprofloxacin Test Discs Due to Labeling Error

    Remel Inc is recalling Oxoid Ciprofloxacin test discs because boxes labeled CIP5 may contain AMP5 cartridges.

    Product
    Oxoid Antimicrobial Susceptibility Test Discs, CTO425B Ciprofloxacin CIP 5 mcg, 50 discs per cartridge, 5 cartridges per box. The firm name on the box label is Oxoid Ltd., Basingstoke, UK. Used in the semi-quantitative agar diffusion test method for in vitro susceptibility…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-350-2014·2013-12-25

    Tween Brands Recalls Shine from Within Blueberry Anti-Bac Justice Due to Label Error

    Tween Brands Inc is recalling 25,078 bottles of Shine from Within Blueberry Anti-Bac Justice because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.

    Product
    Shine from within blueberry Anti bac Justice, Ethyl Alcohol, Net Wt 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-353-2014·2013-12-25

    Tween Brands Recalls Hand Sanitizer Due to Alcohol Content Labeling Error

    Tween Brands Inc is recalling 47,343 bottles of hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of the actual 20%.

    Product
    TODAY IS AWESOME! Justice, Cotton Candy anti bac, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·13E071000·2013-12-24

    Meritor Trailer Axle Recall for Potential Wheel Separation Risk

    Meritor is recalling specific remanufactured trailer axles where misaligned parts could cause wheel separation and increase crash risk.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V643000·2013-12-24

    Blue Bird Recalls 2014-2015 School Buses Due to Parking Brake Defect

    Blue Bird is recalling 2014-2015 All American and Vision school buses because a parking brake component may fracture, causing the brake to release unexpectedly.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V645000·2013-12-24

    Nissan Recalls 2014 Titan Trucks for Incorrect Tire Load Labels

    Nissan is recalling 2014 Titan King Cab and Crew Cab trucks because the tire and loading information label overstates the vehicle's maximum load and passenger capacity.

    Product
    NISSAN — NISSAN TITAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V644000·2013-12-24

    Cargo South Recalls Enclosed Utility Trailers Due to Door Lock Defect

    Cargo South is recalling 2006-2013 enclosed utility trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside.

    Product
    CARGO SOUTH — CARGO SOUTH ENCLOSED UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V639000·2013-12-20

    Thomas Built Buses Recalls 2014-2015 Saf-T-Liner EFX School Buses

    Daimler Trucks North America is recalling 45 school buses because an incorrect speedometer calibration may display a lower speed than the vehicle is actually traveling.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13E073000·2013-12-20

    GM Recalls 2014 Trucks for Transmission Software Error

    General Motors is recalling 2014 Chevrolet Silverados and GMC Sierras because incorrect transmission software may fail to display first gear, increasing crash risk.

    Product
    GMC — GMC, CHEVROLET SIERRA, SILVERADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V654000·2013-12-20

    Starcraft Recalls 2014 Comet RVs Due to Incorrect Tire Load Labels

    Starcraft is recalling 50 model year 2014 Comet recreational vehicles because certification labels incorrectly identify tire load ranges, potentially leading to unsafe tire replacements.

    Product
    STARCRAFT — STARCRAFT COMET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V640000·2013-12-20

    Freightliner Recalls MT45, MT55, and MBC Chassis for Speedometer Calibration

    Daimler Trucks North America is recalling 2014 Freightliner chassis because an incorrect speedometer calibration may display a lower speed than actual, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC MT45, MBC, MT55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V646000·2013-12-20

    Riverside Travel Trailer Recall for Door Lock Jamming Risk

    Riverside is recalling 2006-2014 travel trailers with Fastec door locks that may jam, potentially trapping occupants inside the vehicle.

    Product
    RIVERSIDE — RIVERSIDE TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14071·2013-12-20

    Yankee Candle Recalls Pine Berry Candle Ring Due to Fire Hazard

    Yankee Candle is recalling Pine Berry candle rings because their synthetic foliage and berries are flammable, posing a fire hazard. No injuries have been reported.

    Product
    Candle Ring - Pine Berry
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·14069·2013-12-19

    Playtex Recalls Hip Hammock Infant Carriers Due to Fall Hazard

    Playtex is recalling Hip Hammock infant carriers because buckles can crack or break, posing a fall hazard to children.

    Product
    Playtex Hip Hammock infant carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V638000·2013-12-19

    Tiffin Allegro Motorhomes Recalled for Electric Fireplace Fire Risk

    Tiffin is recalling 2013-2014 Allegro 33AA motorhomes because exposed wood in the electric fireplace may ignite, potentially causing the vehicle to catch fire.

    Product
    TIFFIN — TIFFIN ALLEGRO
    Category
    Vehicle
    Distribution
    Distributed nationwide

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