The Recall Desk

Archive

April 2015 recalls

1,319 recalls were announced in April 2015.

What the numbers show

Critical
109
Severe
569
High
350
Moderate
275
Low
16

Of the 1,319 recalls this month scored against our rubric, 8% are Critical, 43% are Severe.

Which agencies issued them

1101–1200 of 1319

  • ModerateFDA (Devices)·Z-1368-2015·2015-04-08

    Quest Medical Recalls Lacrimal Intubation Sets Due to Labeling Error

    Quest Medical is recalling 106 units of LIS27T Lacrimal Intubation Sets because the expiration date was incorrectly printed in the manufacturing date field.

    Product
    LIS27T - Lacrimal Intubation Set RX Only Sterile Used in various ophthalmology procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1348-2015·2015-04-08

    Microtek Medical Recalls Sterile Laser Resistant Wands Due to Latex Packaging

    Microtek Medical Inc is recalling sterile laser resistant wands because the packaging contains latex but lacks the required warning label.

    Product
    LASER RESISTANT WAND - STERILE, 7/8" X 8" (2.22cm x 20.32cm), REF 24013, QTY 10 EA, STERILE EO, NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1754-2015·2015-04-08

    Health One Pharmaceuticals Recalls San Ye Qing Dietary Supplements

    Health One Pharmaceuticals is recalling Complex Tablet San Ye Qing dietary supplements due to significant violations of cGMP regulations.

    Product
    Complex Tablet San Ye Qing, 120 tablets, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1668-2015·2015-04-08

    Health One Pharmaceuticals Recalls In Act Xtract Dietary Supplements

    Health One Pharmaceuticals is recalling In Act Xtract dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    In Act Xtract
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1337-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmet Systems Due to Latex Packaging

    Microtek Medical is recalling 10 Freedomaire Surgical Helmet Systems because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY, LUMBAR BELT AND MOTOR MODULE, REF 11110STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1342-2015·2015-04-08

    Microtek Smoke Evacuation Tubing Set Recalled for Latex Packaging Labeling Error

    Microtek Medical Inc is recalling 303 Smoke Evacuation Tubing Sets because the packaging contains latex but lacks the required warning label.

    Product
    Smoke Evacuation Tubing Set for Coherent CPG Handpiece, 7/8" x 16' (2.22 cm x 487.88 cm), REF 24244, QTY 3/CS, NON STERILE NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1773-2015·2015-04-08

    Health One Pharmaceuticals Recalls Vigerect Dietary Supplements

    Health One Pharmaceuticals is recalling Vigerect dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    Vigerect
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1347-2015·2015-04-08

    Microtek Medical Smoke Evacuator Tube Sets Recalled for Latex Packaging

    Microtek Medical Inc is recalling sterile smoke evacuator tube sets because the packaging contains latex without the required warning label.

    Product
    (S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor, Sterile, REF 24155, QTY 10/CS, STERILE EO, NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1648-2015·2015-04-08

    Health One Pharmaceuticals Recalls Yin Vive Dietary Supplement

    Health One Pharmaceuticals is recalling Yin Vive dietary supplements due to significant violations of cGMP regulations.

    Product
    Yin Vive, 80 Veggie Capsules, 400mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1375-2015·2015-04-08

    BD Biosciences Recalls CD123 PE Reagent Due to Antibody Contamination

    BD Biosciences is recalling one lot of CD123 PE reagent because it contains a low amount of CD4 antibody, which may result in unexpected staining patterns.

    Product
    CD123 (9F5) PE Catalog number 649453 Analyte Specific Reagent
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1360-2015·2015-04-08

    Zimmer Recalls Persona Anterior Referencing Sizers Due to Specification Nonconformance

    Zimmer, Inc. is voluntarily recalling 22 lots of Persona Anterior Referencing Sizers with Locking Boom because the devices do not conform to print specifications.

    Product
    Brand Name: Persona¿ Anterior Referencing Sizer with Locking Boom The Persona Anterior Referencing Sizer is a sterilizable instrument intended for use in multiple total knee arthroplasty procedures. The Persona Surgical Technique (97-5026-001-00, Rev. 9) states that the sizer…
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Food)·F-1673-2015·2015-04-08

    Health One Pharmaceuticals Recalls Shrink & Clean Dietary Supplement

    Health One Pharmaceuticals is recalling Shrink & Clean dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Shrink & Clean, 60 Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1361-2015·2015-04-08

    King Systems Double Swivel Connector Recalled for Mislabeling

    King Systems Corp. is recalling 900 units of Double Swivel Connectors mislabeled as having a suction port. The error may cause a short procedure delay but poses no risk to patients.

    Product
    Double Swivel Connector with Suction Port Connector, Airway (Extension) King Systems part 7169 Product Usage: An airway connector is a device intended to connect a breathing gas source to a tracheal tube, tracheostomy tube, or gas mask. The double swivel connector with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1343-2015·2015-04-08

    Microtek Medical Smoke Evacuator Tubing Recalled for Unlabeled Latex Packaging

    Microtek Medical is recalling smoke evacuator tubing because the packaging contains latex but lacks the required warning label.

    Product
    TUBING 7/8' X 10', W/WAND & TIP, 24/CS, REF 24187, QTY 24\CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1653-2015·2015-04-08

    Health One Recalls True Woman Dietary Supplements for cGMP Violations

    Health One Pharmaceuticals is recalling True Woman dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    True Woman, 60 Vege Capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1374-2015·2015-04-08

    Biologic Therapies Recalls Bio-CORE Cannula Sets for Misbranding

    Biologic Therapies, Inc. is recalling Bio-CORE Cannula (Needle) Sets because they were distributed without proper FDA clearance and classification.

    Product
    Bio-CORE Cannula (Needle) Set
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·F-1679-2015·2015-04-08

    Health One Pharmaceuticals Recalls Griffonia Seed Extract 5-HTP Capsules

    Health One Pharmaceuticals is recalling Griffonia Seed Extract 5-HTP Capsules due to significant violations of cGMP regulations for dietary supplements.

    Product
    Griffonia Seed Extract 5-HTP Capsule, 60 capsules, 100mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1718-2015·2015-04-08

    Health One Pharmaceuticals Recalls Fish Oil 200 for cGMP Violations

    Health One Pharmaceuticals is recalling Fish Oil 200 dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Fish Oil 200
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1744-2015·2015-04-08

    Health One Pharmaceuticals Recalls Passion Secret Dietary Supplements

    Health One Pharmaceuticals is recalling Passion Secret dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Passion Secret
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1671-2015·2015-04-08

    Health One Pharmaceuticals Recalls Four Things Combination Dietary Supplement

    Health One Pharmaceuticals is recalling Four things Combination dietary supplements due to significant violations of current good manufacturing practices (cGMP) regulations.

    Product
    Four things Combination, 100 Vegetarian Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1366-2015·2015-04-08

    Owen Mumford Autoject E1 Fixed Needle Device Recalled for Missing Components

    Owen Mumford USA, Inc. is recalling 3,100 Autoject E1 Fixed needle devices because the syringe carrier is missing a damper and spring.

    Product
    Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by patients to inject drugs as prescribed by their doctor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1658-2015·2015-04-08

    Health One Pharmaceuticals Recalls Protein Mix for cGMP Violations

    Health One Pharmaceuticals is recalling Protein Mix dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Protein Mix
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1353-2015·2015-04-08

    Stryker Recalls Vitagel Surgical Hemostat Due to Cold Chain Violations

    Stryker Orthobiologics is recalling Vitagel surgical hemostat shipments that were not delivered within validated timeframes, potentially compromising the product's required cold storage.

    Product
    Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1660-2015·2015-04-08

    Health One Pharmaceuticals Recalls Herbal Health Dietary Supplements

    Health One Pharmaceuticals is recalling Herbal Health dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Herbal Health
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1358-2015·2015-04-08

    Bard Urinary Drainage Bags Recalled for Potential Sterile Barrier Breach

    C.R. Bard is recalling specific lots of urinary drainage bags due to a potential breach of the sterile barrier packaging.

    Product
    Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot # NGYJ0603 and NGYJ1671
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1349-2015·2015-04-08

    Microtek Medical recalls sterile smoke evacuator wands due to latex packaging

    Microtek Medical is recalling sterile smoke evacuator wands because the packaging contains latex but lacks the required warning label.

    Product
    INTEGRAL WAND W/TUBING, STERILE, REF 24185, QTY 24/CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms, Trauma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1783-2015·2015-04-08

    ProSupps Recalls MR. Hyde Pre-Workout for Undeclared Yohimbine Levels

    ProSupps USA LLC is recalling MR. Hyde Intense Energy Pre Workout because it contains more yohimbine HCL than declared on the label.

    Product
    MR. HYDE INTENSE ENERGY PRE WORKOUT, Green Apple Natural and Artificial Flavor Dietary Supplement Net Weight 8.0 OZ (228 grams)
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1352-2015·2015-04-08

    Synthes Aiming Arms Recalled Due to Potential Jamming of Guide Sleeve

    Synthes, Inc. is recalling 131 Aiming Arms from the TFN-ADVANCED system because the guide sleeve may jam, potentially delaying instrument removal.

    Product
    Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm; The 130 Degree Aiming Arm and 125 Degree Aiming Arm are a part of the TFN-ADVANCED (TFNA) System. The TFN-ADVANCED Proximal Femoral Nailing System is intended for treatment of fractures in adults and adolescents (12-21)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1676-2015·2015-04-08

    Health One Pharmaceuticals Recalls Reishi Spore Gen Dietary Supplements

    Health One Pharmaceuticals is recalling Reishi Spore Gen dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Reishi Spore Gen, 90 Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1340-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmets Due to Latex Packaging

    Microtek Medical Inc is recalling 11 units of Freedomaire Surgical Helmet Systems because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET SYSTEM WITH BELT, REF 11114STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical personnel in order to protect against…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1367-2015·2015-04-08

    Nidek YC-1800 Ophthalmic YAG Laser System Recalled for Pitting Lens

    Nidek Inc is recalling 799 YC-1800 Ophthalmic YAG Laser Systems due to complaints of pitting lenses that may cause unclear images.

    Product
    YC-1800 OPHTHALMIC YAG LASER SYSTEM; The YC-1800 allows the safe and bloodless treatment of intraocular diseases for outpatients by mechanical disruption caused by energy of the YAG laser pulses.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1764-2015·2015-04-08

    Health One Pharmaceuticals Recalls Super pill#2 Dietary Supplements

    Health One Pharmaceuticals is recalling Super pill#2 dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    Super pill#2
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1708-2015·2015-04-08

    Health One Pharmaceuticals Recalls Cholesterol Formula Due to cGMP Violations

    Health One Pharmaceuticals is recalling Cholesterol Formula capsules due to significant violations of current Good Manufacturing Practice (cGMP) regulations for dietary supplements.

    Product
    Cholesterol Formula, 90 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1345-2015·2015-04-08

    Microtek Medical Recalls Sterile Vacuum Tubing Due to Unlabeled Latex Packaging

    Microtek Medical Inc is recalling sterile vacuum tubing because the packaging contains latex but lacks the required warning label.

    Product
    VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm), WITH TUBING EXTENDER, STERILE, REF 24010, QTY 24\CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1675-2015·2015-04-08

    Health One Recalls Siberian Ginseng Supplements for cGMP Violations

    Health One Pharmaceuticals is recalling 199 units of Siberian Ginseng supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Siberian Ginseng, 100 capsules, 500 mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1339-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmets Due to Latex Packaging

    Microtek Medical Inc is recalling 153 Freedomaire Surgical Helmets because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET WITH MOTOR MODULE, REF 11113STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical personnel in order to protect against…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1636-2015·2015-04-08

    Health One Pharmaceuticals Recalls Bone Essense Dietary Supplement

    Health One Pharmaceuticals is recalling Bone Essense, 60 capsules, due to significant violations of cGMP regulations for dietary supplements.

    Product
    Bone Essense, 60 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1749-2015·2015-04-08

    Health One Pharmaceuticals Recalls Protein Powder for cGMP Violations

    Health One Pharmaceuticals is recalling Protein Powder due to significant violations of current Good Manufacturing Practice (cGMP) regulations for dietary supplements.

    Product
    Protein Powder
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1767-2015·2015-04-08

    Health One Pharmaceuticals Recalls U O Clear Dietary Supplements

    Health One Pharmaceuticals is recalling U O Clear dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    U O Clear
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1344-2015·2015-04-08

    Microtek Medical Recalls Vacuum Tubing Due to Unlabeled Latex Packaging

    Microtek Medical Inc is recalling non-sterile vacuum tubing because the packaging contains latex but lacks the required warning label.

    Product
    VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm), REF 24009, QTY 24\CS, NON-STERILE Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1768-2015·2015-04-08

    Health One Pharmaceuticals Recalls Ultra Lecithin Dietary Supplements

    Health One Pharmaceuticals is recalling Ultra Lecithin dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Ultra Lecithin
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1365-2015·2015-04-08

    Medtronic Recalls Trellis 6 and 8 Peripheral Infusion Systems for Sterility Breach

    Medtronic is voluntarily recalling Trellis 6 and 8 Peripheral Infusion Systems due to potential sterility breaches in the outer packaging.

    Product
    Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V01, BVT608030V01, BVT612010V01, BVT612030V01, CVT808015, CVT808025, CVT812015, CVT812025, EVT808015, EVT808025, EVT812015, EVT812025, BVT808015, BVT808030, BVT812015, BVT812030…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1706-2015·2015-04-08

    Health One Pharmaceuticals Recalls Cardiospecs Dietary Supplements

    Health One Pharmaceuticals is recalling Cardiospecs dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    Cardiospecs
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1354-2015·2015-04-08

    Siemens Syngo.plaza PACS Recalled for Incomplete Archived Studies

    Siemens Medical Solutions is recalling four Syngo.plaza PACS units because they may leave partially archived studies unarchived during pre-fetch operations.

    Product
    Syngo.plaza. A Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and treatment planning.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Food)·F-1688-2015·2015-04-08

    Health One Pharmaceuticals Recalls Gamma Zyme Dietary Supplements

    Health One Pharmaceuticals is recalling Gamma Zyme dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Gamma Zyme, 100 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1753-2015·2015-04-08

    Health One Recalls Reishi Mushroom Capsules for cGMP Violations

    Health One Pharmaceuticals is recalling Reishi Mushroom capsules due to significant violations of dietary supplement manufacturing regulations.

    Product
    Reishi Mushroom, 90 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1633-2015·2015-04-08

    Health One Pharmaceuticals Recalls Shu Chang Bao Dietary Supplements

    Health One Pharmaceuticals is recalling Shu Chang Bao dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Shu Chang Bao, 150 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1738-2015·2015-04-08

    Health One Pharmaceuticals Recalls Motichi Dietary Supplements

    Health One Pharmaceuticals is recalling Motichi dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Motichi
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1785-2015·2015-04-08

    French Broad Chocolates Recalls Bubbie's Almond Bar Due to Cacao Moth

    French Broad Luscious Chocolates is recalling Bubbie's Almond Bars because of the presence of a cacao moth in the almonds.

    Product
    French Broad Chocolates, Bubbie's Almond Bar, 60g (2.1 oz) bar, with aluminum foil with polyester ribbon & paper outer wrapper
    Category
    Food
    Distribution
    7 states
  • LowFDA (Food)·F-1805-2015·2015-04-08

    Cheryl's Bunny Head Cookies Recalled for Incorrect Packaging Film

    Cheryl's is recalling Buttercream Frosted Cut-Out Bunny Head Cookies because they were packed in film lacking the ingredient cocoa.

    Product
    Cheryl's Buttercream Frosted Cut-Out BUNNY HEAD COOKIES, Net Wt 1.5oz (43g), Cheryl's Westerville, Ohio 43082 www.Cheryls.com ALLERGEN STATEMENT: Contains Wheat, Soy, Milk and Eggs. Produced in a plant that also handles peanuts and tree nuts.
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·15E029000·2015-04-07

    Lippert Trailer Axle Hubs Recalled for Wheel Stud Failure Risk

    Lippert Components is recalling specific trailer axle hubs because wheel mounting studs may fail, potentially causing wheel separation and a crash.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide

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