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.

601–700 of 1402

  • HighFDA (Devices)·Z-0484-2014·2013-12-18

    Trumpf Medical Systems Recalls Helion S and H300 Exam Lights

    Trumpf Medical Systems is recalling 287 Helion S and H300 exam lights because a plastic joint may fail due to fatigue after seven years of use.

    Product
    Helion S Exam Light or H300 The device is intended to locally illuminate an examination area of the patient's body with high intensity light in a clinic or doctor's practice.
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0457-2014·2013-12-18

    Hospira Recalls Receptal Canisters Due to Suction Failure

    Hospira is recalling 1L Receptal Canisters because the canister and liner may not seat properly, preventing the creation of necessary suction.

    Product
    Product is labeled in part: LIST NO. 43449; RECEPTAL CANISTER; DO NOT FILL 900 ABOVE THIS LINE; Product of China; Hospira, Inc.,; Lake Forest, IL 60045 USA. Used to isolate suction waste during surgeries, or to clear patient airways, throat or wounds to allow treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0460-2014·2013-12-18

    Zimmer NexGen Porous Patella Drill Guide Recall Expansion

    Zimmer, Inc. is expanding a recall of NexGen Porous Patella Drill Guides to prevent inadvertent use during surgery, which could cause delays.

    Product
    NexGen Complete Knee Solution Porous Patella Drill Guide-29mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0464-2014·2013-12-18

    Centurion Sterile Rubber Bands Recalled for Contradictory Latex Labeling

    Centurion Medical Products is recalling sterile rubber bands that are labeled as both latex-free and containing natural rubber latex, posing a risk to users with latex allergies.

    Product
    Centurion Sterile # 84 Rubber Bands Reorder EB84, Caution: This product contains natural rubber latex which may cause allergic reactions. LATEX FREE , CAUTION: FEDERAL lAW (USA) RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN Single Use Only bands items…
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0479-2014·2013-12-18

    Aesculap GNI161 Bipolar Foot Control Recalled for Energy Failure

    Aesculap, Inc. is recalling 85 GNI161 Bipolar Foot Controls because the bipolar energy did not stop after the foot control was released.

    Product
    Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar Coagulator is intended for use in surgery to generate electrical power for bipolar instruments. Bipolar coagulators are used in neurosurgery, ENT surgery, urology, laparoscopy, and plastic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V629000·2013-12-18

    CM and S&H Trailers Recalled for Door Lock Jamming Hazard

    Contract Manufacturer, LLC is recalling 2006-2012 CM and S&H trailers because a door lock defect could jam the deadbolt, trapping occupants inside.

    Product
    CM TRAILERS — CM TRAILERS, S&H REVOLUTION, LEGACY, NOMAD, REVOLUTION 2+1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0461-2014·2013-12-18

    Zimmer NexGen Knee Implant Components Recalled for Surgical Delay Risk

    Zimmer, Inc. is recalling 638 NexGen Complete Knee Solution provisional articular surface devices. The recall is an expansion of a previous action to prevent inadvertent use of associated instruments.

    Product
    NexGen Complete Knee Solution CR Articular Surface Provisional-Purple 9mm Height Nonsterile Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic loss of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0459-2014·2013-12-18

    Zimmer NexGen Porous Patella Drill Guide Recall Expansion

    Zimmer, Inc. is expanding a recall of NexGen Porous Patella Drill Guides to include five additional instruments. These devices may be inadvertently used during surgery, causing delays.

    Product
    NexGen Complete Knee Solution Porous Patella Drill Guide-26mm dia./10mm thickness Non sterile, Rx Only Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0478-2014·2013-12-18

    Steris Recalls AMSCO Evolution Steam Sterilizer Transfer Carriages

    Steris Corporation is recalling 936 AMSCO Evolution steam sterilizer transfer carriages because they may unlatch when overloaded or maneuvered with excessive force.

    Product
    AMSCO¿ Evolution¿ steam sterilizer Transfer Carriage. Product Usage: Mobile, wheeled transportation unit utilized to carry, load, & unload the Loading Car into and out of steam sterilizer units.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0463-2014·2013-12-18

    Zimmer NexGen Knee Instruments Recalled Due to Potential Surgical Delay

    Zimmer, Inc. is recalling five NexGen Micro knee instruments because they may be used incorrectly, causing surgical delays.

    Product
    NexGen Complete Knee Solution CR Articular Surface Provisional-Striped Green 9mm Height Nonsterile Devices are used in total knee arthroplasty and indicated for patients with severe pain and disability due to conditions such as arthritis, collagen disorders, post-traumatic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0480-2014·2013-12-18

    Zimmer Recalls NexGen Knee Components Due to Stem Locking Failure

    Zimmer, Inc. is recalling 128 NexGen Complete Knee Solutions Stemmed Tibial Components because the stem may not lock into the tibia.

    Product
    NexGen¿ Complete Knee Solutions Stemmed Tibial Component Precoat NexGen Tibial Baseplates are part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis. The device is indicated for patients with severe knee pain and disability due to: Rheumatoid…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V636000·2013-12-18

    Altec Digger Derrick Recall for Loose Feeder Tube Bracket Fasteners

    Altec is recalling 2009-2013 Digger Derrick models because loose fasteners may allow the feeder tube to fall, posing an injury risk to nearby people.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-340-2014·2013-12-18

    Novartis Recalls Tekturna HCT Physician Samples Due to Chemical Contamination

    Novartis is recalling Tekturna HCT physician sample bottles due to contamination with Darocur 1173, a photo curing agent used in ink.

    Product
    Tekturna HCT (aliskiren and hydrochlorothiazide) Tablets 300/25 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only, Manufactured by: Novartis Pharma Productions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-343-2014·2013-12-18

    Oxcarbazepine Tablets Recalled for Potential Subpotency

    Boehringer Ingelheim Roxane Inc. is recalling Oxcarbazepine Tablets, 150 mg, due to out-of-specification assay results and potential lower weight tablets.

    Product
    Oxcarbazepine Tablets, 150 mg, packaged in a) 10 x 10 count Unit-Dose Tablets in blisters packaged in a carton (NDC 0054-0097-20) and b) 100-count bottle (NDC 0054-0097-25), Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0465-2014·2013-12-18

    Karl Storz Recalls Misidentified Axillent Debakey Grasping Forceps

    Karl Storz is recalling 7 units of Axillent Debakey Grasping Forceps because they were mislabeled as a different model.

    Product
    Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey forceps to grasp tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-329-2014·2013-12-18

    Novartis Recalls Exforge Physician Samples Due to Chemical Contamination

    Novartis is recalling Exforge physician sample bottles due to contamination with Darocur 1173, a photocuring agent used in ink.

    Product
    Exforge (amlodipine and valsartan Tablets) 5/320 mg, Rx only 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936 - NDC # 0078-9490-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-331-2014·2013-12-18

    Novartis Recalls Multiple Prescription Medications Due to Chemical Contamination

    Novartis is recalling physician sample bottles of several prescription medications due to contamination with a photocuring agent found in ink.

    Product
    Exforge HCT (amlodipine, valsartan, hydrochlorothiazide) 5/160/12.5 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0469-2014·2013-12-18

    Omnyx Digital Pathology Software Recalled for Incorrect Measurement Display

    Omnyx LLC is recalling Digital Pathology System (DPS) Software version 1.1 because its annotation tools may display incorrect measurements and area calculations for regions of interest on scanned slides.

    Product
    Digital Pathology System (DPS) Software version 1.1 The Omnyx" Integrated Digital Pathology system, which consists of a whole slide scanner and associated software applications, is a scanning, receiving, storing, managing, annotating and computer monitor viewing system for…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-337-2014·2013-12-18

    Novartis Recalls Physician Sample Tablets Due to Chemical Contamination

    Novartis is recalling physician sample bottles of several prescription medications, including Tekturna, due to contamination with a photocuring agent.

    Product
    Tekturna (aliskiren) Tablets 150 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only. Manufactured by: Novartis Pharma Productions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9485-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-327-2014·2013-12-18

    Novartis Recalls Diovan and Other Tablets Due to Chemical Contamination

    Novartis is recalling physician sample bottles of Diovan and other tablets because they were contaminated with Darocur 1173, a photocuring agent used in inks.

    Product
    Diovan (valsartan) 320 mg per tablet, 7 Tablets per bottle, Rx only Physician Sample Not For Sale, Manufactured by: Novartis Pharmaceuticals Corporation Suffern, NY 10901 for Novartis Pharmaceuticals Corporation East Hanover, NJ 07936, NDC # 0078-9360-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-328-2014·2013-12-18

    Novartis Recalls Exforge Physician Samples Due to Chemical Contamination

    Novartis is recalling Exforge physician sample bottles due to contamination with Darocur 1173, a photocuring agent found in ink.

    Product
    Exforge (amlodipine and valsartan Tablets) 5/160 mg, Rx only 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936 - NDC # 0078-9488-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0482-2014·2013-12-18

    Accumetrics Recalls VerifyNow IIb/IIIa Test Kits Due to Incorrect Instructions

    Accumetrics is recalling VerifyNow IIb/IIIa Test Kits because they contain incorrect instructions regarding the time limit for performing the test after sample collection.

    Product
    VerifyNow IIb/IIIa Test, 10-Test Kit, Catalog No. 85310, 10 tests/box; 690 total tests. The VerifyNow IIb/IlIa Test is a semi-quantitative, whole blood platelet function test used to measure glycoprotein (GP) lIb/IlIa receptor blockade in patients treated with abciximab or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0817-2014·2013-12-18

    Sugar-Free Carrot Cake Recalled for Missing Phenylketonuria Warning

    Cakes & More Delight's is recalling sugar-free carrot cakes because they contain aspartame but lack the required phenylketonuria warning.

    Product
    Sugar free cake: Carrot flavor, Package size: 4 oz, 12 oz.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0822-2014·2013-12-18

    Sugar-Free Almond Cake Recalled for Missing Phenylketonuria Warning

    Cakes & More Delight's is recalling sugar-free almond cakes because the packaging lacks a required warning for individuals with phenylketonuria (PKU).

    Product
    Sugar free cake: Almond flavor. Package size:12 oz
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0467-2014·2013-12-18

    Stryker Recalls Accolade II Hip Stems Due to Packaging Error

    Stryker is recalling 20 Accolade II Hip Stems because a Size #3 was found packaged with a Size #5. The error poses a risk of incorrect implant selection.

    Product
    1) Accolade II 127 Neck Angle Hip Stem, Size # 3 2) Accolade II 127 Neck Angle Hip Stem, Size #5 Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA Telephone # +1 201-831-5000 Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0471-2014·2013-12-18

    Beckman Coulter Recalls LH 750 and LH 780 Hematology Systems

    Beckman Coulter is recalling LH 750 and LH 780 Hematology Systems because optical degradation may delay reporting results for specific blood cell counts.

    Product
    Coulter LH 780 Hematology Analyzer, Part No. 723585, A90728 Product Usage: Coulter LH 780 Hematology Analyzer is a is a quantitative, automated hematology analyzer and leukocyte differential counter For In Vitro Diagnostic Use in clinical laboratories. The Coulter¿ LH 780…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0474-2014·2013-12-18

    Synthes Trochanteric Fixation Nail Recalled for Incorrect Packaging Labeling

    Synthes USA is recalling 12 Trochanteric Fixation Nails because the packaging incorrectly lists the nail's length and diameter.

    Product
    Synthes Trochanteric Fixation Nail As part of the Synthes Trochanteric Fixation Nail (TFN) System, the TFN Nail is intended to treat stable and unstable fractures of the proximal femur.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0475-2014·2013-12-18

    Zimmer Trabecular Metal Total Ankle Talar Component Recall for Residue

    Zimmer, Inc. is recalling specific Total Ankle Talar Components because routine monitoring found potential elevated levels of manufacturing residue on the implants.

    Product
    Zimmer Trabecular Metal Total Ankle Talar Component Left Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobility by restoring alignment, reducing pain and preserving the flexion/extension movement within the ankle joint.The Zimmer Trabecular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-346-2014·2013-12-18

    Lupin Recalls Ethambutol Hydrochloride Tablets Due to Impurity

    Lupin Pharmaceuticals is recalling 4,896 bottles of Ethambutol Hydrochloride 400 mg tablets because of an out-of-specification impurity result.

    Product
    ETHAMBUTOL HYDROCHLORIDE — ETHAMBUTOL HYDROCHLORIDE (ETHAMBUTOL HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-338-2014·2013-12-18

    Novartis Recalls Tekturna Tablets Due to Chemical Contamination

    Novartis is recalling Tekturna physician sample bottles contaminated with Darocur 1173, a photocuring agent found in ink.

    Product
    Tekturna (aliskiren) Tablets 300 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only. Manufactured by: Novartis Pharma Produktions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9486-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-334-2014·2013-12-18

    Novartis Recalls Exforge Physician Samples Due to Chemical Contamination

    Novartis is recalling Exforge physician sample bottles due to contamination with Darocur 1173, a photocuring agent found in ink.

    Product
    Exforge (amlodipine and valsartan, Tablets) 10/320 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9491-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0473-2014·2013-12-18

    Synthes TomoFix Osteotomy System Recalled for Surgical Technique Guide Labeling Error

    Synthes USA HQ, Inc. is recalling the TomoFix Osteotomy System due to a labeling error in the Surgical Technique Guide that may cause surgical delays.

    Product
    Synthes TomoFix Plates The Synthes J5606-C TomoFix Osteotomy System is used for open and closed wedge osteotomies of the medial proximal tibia, lateral proximal tibia, medial and lateral distal femur, treatment of bone and joint deformities, fractures, and malalignment caused…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0483-2014·2013-12-18

    Stryker Recalls Cancellous Bone Screws Due to Packaging Error

    Stryker is recalling specific Cancellous Bone Screws because a 5.5 mm screw was found in packaging labeled for a 6.5 mm screw.

    Product
    Stryker Orthopaedics Cancellous Bone Screw Howmedica Osteonics Corp. Stryker France Both the 6.4 mm diameter, 25mm length, Cancellous Bone Screws (Cat no 2030-6525-1) and the 5.5mm diameter, 40 mm length Cancellous Bone Screws (Cat no 2029-5540-1) are cleared for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0821-2014·2013-12-18

    Sugar-Free Corn Cake Recalled for Missing Phenylketonuria Warning

    Cakes & More Delight's is recalling sugar-free corn cakes because the packaging lacks a warning for individuals with phenylketonuria (PKU). The product contains aspartame.

    Product
    Sugar free cake: Corn. Package size: 4 oz, 12 oz
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-330-2014·2013-12-18

    Novartis Recalls Physician Sample Blood Pressure Medications Due to Chemical Contamination

    Novartis is recalling physician sample bottles of several blood pressure and cholesterol medications due to contamination with a photocuring agent used in packaging inks.

    Product
    Exforge HCT (amlodipine, valsartan, hydrochlorothiazide) 10/320/25 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-339-2014·2013-12-18

    Novartis Recalls Tekturna HCT Physician Samples Due to Chemical Contamination

    Novartis is recalling physician sample bottles of Tekturna HCT and other medications due to contamination with Darocur 1173, a photo-curing agent.

    Product
    Tekturna HCT (aliskiren and hydrochlorothiazide) Tablets 150/12.5 mg, 7 tablets per bottle, Physician Sample-Not For Sale, Rx only, Manufactured by: Novartis Pharma Productions GmbH Wehr, Germany. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-333-2014·2013-12-18

    Novartis Recalls Physician Sample Blood Pressure Medications Due to Chemical Contamination

    Novartis is recalling physician sample bottles of several blood pressure medications due to contamination with a photocuring agent found in packaging inks.

    Product
    Exforge (amlodipine and valsartan Tablets) 10/160 mg, Rx only, 7 tablets per bottle, Physician Sample - Not For Sale. Manufactured by: Novartis Pharma Stein AG Stein, Switzerland. Distributed by: Novartis Pharmaceuticals Corp. East Hanover, New Jersey 07936, NDC # 0078-9489-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-347-2014·2013-12-18

    Taro Recalls Subpotent Ciclopirox Shampoo 1% Prescription Bottles

    Taro Pharmaceuticals is recalling 850 bottles of Ciclopirox Shampoo 1% because the product is subpotent. The recall is voluntary and nationwide.

    Product
    CICLOPIROX — CICLOPIROX (CICLOPIROX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0481-2014·2013-12-18

    Ultradent Recalls Avex CX2 Ceramic Orthodontic Brackets Due to Design Control Issues

    Ultradent is recalling 217 units of Avex CX2 Ceramic Orthodontic Brackets because the design control process was not completed before distribution.

    Product
    Opal Orthodontics by Ultradent. Avex CX2 Ceramic Orthodontic Brackets Avex CX2 ceramic brackets are intended for use in orthodontic treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0819-2014·2013-12-18

    Cakes & More Delight's Recalls Sugar-Free Vanilla Cakes for Missing Warning

    Cakes & More Delight's is recalling sugar-free vanilla cakes because they contain aspartame but lack the required phenylketonuria warning.

    Product
    Sugar free cake: Vanilla flavor. Package size: 4 oz, 12 oz; Sliced Sugar-free cake: Vanilla flavor 16 oz.
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·13V627000·2013-12-17

    Freightliner Recalls 2013-2014 Cascadia Trucks Due to Wiring Defect

    Daimler Trucks North America is recalling 2013-2014 Freightliner Cascadia trucks because reversed wiring may reduce traction and parking brake effectiveness.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14061·2013-12-17

    HP Chromebook 11 Chargers Recalled for Fire and Burn Hazards

    Google and HP are recalling HP Chromebook 11 chargers because they can overheat and melt, posing fire and burn risks.

    Product
    HP Chromebook 11 power supply/charger
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V626000·2013-12-17

    CJay Trailers Recall Cargo Trailers Due to Door Lock Jamming Risk

    CJay is recalling specific cargo trailers because a defect in the door lock may jam the deadbolt, potentially trapping occupants inside the trailer.

    Product
    CJAY — CJAY CJ714, CJ814, CJ716, CJ820
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V625000·2013-12-17

    Monaco Recalls 2008-2013 RVs With Potential Door Lock Jamming Defect

    Monaco RV is recalling 3,175 recreational vehicles because a door lock defect may jam the deadbolt, potentially trapping occupants inside.

    Product
    MCKENZIE — MCKENZIE, R-VISION, HOLIDAY RAMBLER ION, SILVER CREEK, TRAIL CRUISER CLASSIC, TRAIL LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V633000·2013-12-16

    Thomas Built Saf-T-Liner C2 School Bus Recall for Transmission Software

    Daimler Trucks North America is recalling 2011-2013 Thomas Built Saf-T-Liner C2 school buses because transmission software may cause unintended acceleration.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES, THOMAS BUILT SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V624000·2013-12-16

    Hyundai Recalls 2014 Santa Fe Vehicles Due to Tire Sidewall Defect

    Hyundai is recalling 2014 Santa Fe vehicles equipped with specific Continental tires that may have damaged sidewalls, increasing the risk of tread detachment or rapid air loss.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V622000·2013-12-16

    Honda Recalls 2014 Acura RLX for Rear Suspension Bolt Issues

    Honda is recalling 7,387 2014 Acura RLX vehicles because rear suspension bolts may have loosened, potentially reducing steering ability and increasing crash risk.

    Product
    ACURA — ACURA RLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V634000·2013-12-16

    Freightliner Trucks Recalled for Transmission Software Defect

    Daimler Trucks North America is recalling 2009-2014 Freightliner trucks because transmission software may cause unintended acceleration.

    Product
    FREIGHTLINER — FREIGHTLINER MT45, BUSINESS CLASS M2, MT55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V623000·2013-12-16

    Hino Recalls 2013 NV8J Trucks for Incorrect Weight Documentation

    Hino is recalling 2013 NV8J trucks because vehicle documents show a higher weight rating than the actual modified rating, which could lead to overloading.

    Product
    HINO — HINO NV8J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14059·2013-12-16

    Wahl Recalls Total Care Aerosol Cleaner Due to Burn Hazard

    Wahl is recalling Total Care aerosol cleaner because vapors can ignite near hair clippers, posing a burn hazard. Three incidents were reported, including one minor burn.

    Product
    Total Care, Aerosol Cleaner, Lubricant & Coolant
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13T012000·2013-12-12

    Michelin Recalls LTX M/S Tires Due to Tread Separation Risk

    Michelin is recalling specific LTX M/S tires due to a risk of tread separation that could lead to loss of vehicle control.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14054·2013-12-12

    Coby 32-inch Flat Screen Televisions Recalled for Fire and Burn Hazards

    Thirteen retailers are recalling about 8,900 Coby 32-inch flat screen televisions because an electronic component can fail, catch fire, and ignite nearby items.

    Product
    Coby 32-inch flat screen televisions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V616000·2013-12-12

    Double R Utility Trailers Recalled for Door Lock Jamming Hazard

    Double R is recalling 2010-2014 utility trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside.

    Product
    DOUBLE R TRAILERS — DOUBLE R TRAILERS UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14055·2013-12-12

    Trek Recalls 2013 Madone Bicycles Due to Front Brake Failure Hazard

    Trek is recalling 6,800 model year 2013 Madone bicycles because the front brake can fail, posing a crash hazard. No injuries have been reported.

    Product
    Trek model year 2013 Madone bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13E070000·2013-12-12

    Genera Recalls Aftermarket Tail Lights for 2012-2013 Toyota Prius V

    Genera Corporation is recalling aftermarket tail lights for 2012-2013 Toyota Prius V vehicles because the brake and tail light circuits are switched, reducing the ability to warn other drivers.

    Product
    TOYOTA — TOYOTA PRIUS V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0554-2014·2013-12-11

    Garden-Fresh Foods Recalls D'Amico Tortellini Salad Due to Listeria Risk

    Garden-Fresh Foods is recalling D'Amico & Sons Tortellini Salad products because they may be contaminated with Listeria monocytogenes.

    Product
    D'Amico & Sons Tortellini Salad, Product Code 0 85239 10128 5, 6/6 oz D'Amico & Sons Tortellini Salad, Product Code 0 85239 12700 1, 6/14 oz
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0505-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Roasted Garlic Potato Salad, Product Code 10 733147 10159 6,1/8 lb;
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0650-2014·2013-12-11

    Garden-Fresh Foods Recalls Pistachio Whip Due to Listeria Risk

    Garden-Fresh Foods is recalling Finest Traditions Pistachio Whip and other ready-to-eat products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Pistachio Whip, Product Code 10 733147 00020 ,1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0549-2014·2013-12-11

    Garden-Fresh Recalls Spinach Pasta Salad Base Due to Listeria Risk

    Garden-Fresh Foods is recalling Spinach Pasta Salad Base because it may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Spinach Pasta Salad Base, Product Code 0 11596 62072 5,1/5.25lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0564-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Our Own Garden Pasta Salad, Product Code 0 11596 52153 4, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0641-2014·2013-12-11

    Garden-Fresh Foods Recalls Pumpkin Mousse Due to Listeria Contamination Risk

    Garden-Fresh Foods is recalling specific varieties of Pumpkin Mousse because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Pumpkin Mousse, Product Code 0 11596 55053 4, 1/5 lb; Finest Traditions Pumpkin Mousse, Product Code 0 00 11596 55053 4 10/30/2013 - 11/13/2013 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0608-2014·2013-12-11

    Garden-Fresh Recalls Seafood Pasta Salad Due to Listeria Risk

    Garden-Fresh Foods is recalling Seafood Pasta Salad and other ready-to-eat products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Seafood Pasta Salad, 0 11596 55007 7, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0519-2014·2013-12-11

    Garden-Fresh Recalls Market Pantry Macaroni Salad Due to Listeria Risk

    Garden-Fresh Foods is recalling Market Pantry Reduced Fat Macaroni Salad because it may be contaminated with Listeria monocytogenes.

    Product
    Market Pantry Reduced Fat Macaroni Salad, Product Code 0 85239 20118 3, 6/16 oz.
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0517-2014·2013-12-11

    Garden-Fresh Foods Recalls Macaroni Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Family Style Macaroni Salad, Product Code 0 11596 52060 5, 2/5 lb; Garden-Fresh Macaroni Salad,Product Code 0 11596 52005 6, 2/5 lb; Garden-Fresh Macaroni Salad, Product Code 0 11596 14018 6, 12/16 oz; Garden-Fresh Macaroni Salad, Product Code 0 11596 24210 1, 8/2 lb…
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0512-2014·2013-12-11

    Garden-Fresh Foods Recalls Potato Salad Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Our Own Homestyle Mustard Potato Salad, Product Code 0 11596 51047 7, 4/5 lb; ;
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0412-2014·2013-12-11

    Boston Salads Recalls Seafood and Shrimp Salad for Listeria Risk

    Boston Salads & Provisions Co., Inc. is recalling Seafood and Shrimp Salad due to possible Listeria monocytogenes contamination.

    Product
    Seafood and Shrimp Salad packaged in 5 lb Sold under the label: Boston Salads
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0617-2014·2013-12-11

    Garden-Fresh Foods Recalls Smoked Salmon Dip for Listeria Risk

    Garden-Fresh Foods is recalling Archer Farms Smoked Salmon Dip and other ready-to-eat products due to potential Listeria monocytogenes contamination.

    Product
    Archer Farms Smoked Salmon Dip, Product Code 0 85239 99019 3, 6/11 oz
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0559-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads and Dips for Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Garden Vegetable Spaghetti, Product Code 10 733147 10196 1, 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0526-2014·2013-12-11

    Garden-Fresh Foods Recalls Venetian Bow Tie Pasta Due to Listeria Risk

    Garden-Fresh Foods is recalling specific varieties of Venetian Bow Tie Pasta because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Venetian Bow Tie Pasta, Product Code 0 11596 52027 8, 1/5 lb; Dairy Fresh Venetian Bow Tie Pasta, Product Code 0 11596 50042 3 ,1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0652-2014·2013-12-11

    Garden-Fresh Foods Recalls Cheesecake Delight Due to Listeria Risk

    Garden-Fresh Foods is recalling Our Own Cheesecake Delight products because they may be contaminated with Listeria monocytogenes.

    Product
    Our Own Cheesecake Delight , Product Code 0 11596 85066 5, 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0569-2014·2013-12-11

    Garden-Fresh Recalls Reduced Fat Cole Slaw Due to Listeria Risk

    Garden-Fresh Foods is recalling specific varieties of reduced fat cole slaw because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Reduced Fat Cole Slaw, Product Code 0 11596 53202 8, 1/5 lb Garden-Fresh Reduced Fat Cole Slaw, Product Code 0 11596 53500 5, 4/5 lb; Market Pantry Reduced Fat Cole Slaw, Product Code 0 85239 20117 6, 6/15 oz;
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0609-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Archer Farms Neptune Salad, 0 85239 20242 5, 6/6 oz Archer Farms Neptune Salad, 0 85239 20243 2, 6/14 oz
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0538-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Taco Pasta Salad, Product Code 0 11596 52076 6, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0604-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Shrimp Salad, 0 11596 55100 5, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0591-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Fat Free Bean Salad, Product Code 10 733147 10180 0, 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0579-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads and Slaw Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Homemade-Style Cole Slaw, 7 33147 00025 0, 6/16 oz; Finest Traditions Homemade-Style Cole Slaw, 10 733147 10170 1, 1/8 lb;
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0546-2014·2013-12-11

    Garden-Fresh Recalls Ready-to-Eat Salads Due to Listeria Contamination Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Premium Asiago Pasta Salad,Product Code 0 11596 45624 9, 1/4 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0503-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads for Listeria Contamination

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Knowlans Mandarin Salad Base, Product Code 10 733147 10153 4, 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0555-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Ties & Tomatoes Pasta Salad,10 733147 10686 7, 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0701-2014·2013-12-11

    Townsend Farms and Harris Teeter Organic Berry Blends Recalled for Hepatitis A Risk

    Townsend Farms and Harris Teeter organic berry blends are recalled due to potential Hepatitis A virus contamination linked to an illness outbreak.

    Product
    The Costco product is sold under brand name Townsend Farms Organic Antioxidant Blend - The product is a mix of IQF organic berries, specifically; dark tart cherries, pomegranate arils, strawberries, red raspberries, and blueberries. The product is packaged into plastic bags with…
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0520-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads and Dips for Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Creamy Cheddar Macaroni, Product Code 10 733147 10156 5, 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0558-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads for Listeria Contamination

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Finest Traditions Southwest Taco Pasta Salad,Product Code 10 733147 10287 6, 1/8 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0552-2014·2013-12-11

    Garden-Fresh Foods Recalls Ready-to-Eat Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Wheat Berry Salad,Product Code 0 11596 52118 3, 1/4 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0596-2014·2013-12-11

    Garden-Fresh Recalls Deviled Egg Salad Due to Listeria Risk

    Garden-Fresh Foods is recalling Deviled Egg Salad and other ready-to-eat products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Deviled Egg Salad, Product Code 0 11596 52122, 1/5 lb;
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0537-2014·2013-12-11

    Garden-Fresh Recalls Ready-to-Eat Salads Due to Listeria Contamination Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Cheese Tortellini Salad Toscana,Product Code 0 11596 52075 9, 1/5 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0625-2014·2013-12-11

    Garden-Fresh Recalls Ready-to-Eat Salads Due to Listeria Contamination Risk

    Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Anti Pasto Salad Kit, Product Code 0 11596 65634 2 , 1/6 lb
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-0594-2014·2013-12-11

    Garden-Fresh Foods Recalls Egg Salads Due to Listeria Risk

    Garden-Fresh Foods is recalling specific egg salad products because they may be contaminated with Listeria monocytogenes.

    Product
    Garden-Fresh Egg Salad ,Product Code 0 11596 52022 3, 1/5 lb; Weis Egg Salad , Product Code 0 41497 05365 0 , 1/5 lb; Weis Egg Salad,Product Code 0 11596 55221 7, 1/5 lb
    Category
    Food
    Distribution
    10 states

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