The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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40151–40175 of 40480

  • HighFDA (Devices)·Z-0857-2012·2012-08-08

    Arm and Hammer Spinbrush Toothbrush Recalled for Choking Hazard

    Church & Dwight is recalling 22.783 million Arm and Hammer Spinbrush toothbrushes worldwide due to a potential choking hazard from small parts.

    Product
    Arm and Hammer Spinbrush Dual Action Powered Toothbrush Pro-Clean, various models. Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Devices)·Z-2132-2012·2012-08-08

    Baxter Recalls Peritoneal Dialysis Solution Due to Incorrect Inspection Instructions

    Baxter Healthcare is recalling Extraneal and DIANEAL Low Calcium peritoneal dialysis solutions because a technical service representative provided incorrect instructions for inspecting solution bags.

    Product
    Extraneal and/or DIANEAL LOW CALCIUM Peritoneal Dialysis Solution in Plastic Container, PL-146 used with Automated Peritoneal Dialysis System/Automated PD Set with Cassette; Manufactured for Baxter Healthcare Corporation, Deerfield, IL 60015 U.S.A. The HomeChoice dialysis system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2093-2012·2012-08-08

    Arm and Hammer Spinbrush Pro Clean Sonic Toothbrush Recall for Choking Hazard

    Church & Dwight is recalling 1.744 million Arm and Hammer Spinbrush Pro Clean Sonic Powered Toothbrushes due to a potential small parts choking hazard.

    Product
    Arm and Hammer Spinbrush Pro Clean Sonic Powered Toothbrush Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Devices)·Z-2133-2012·2012-08-08

    Abbott i-Stat EG7 Cartridges Recalled for Inaccurate PCO2 Results

    Abbott Point of Care is recalling 52,750 i-Stat EG7 cartridges because they may produce falsely low PCO2 readings if stored at room temperature for four weeks or longer.

    Product
    I-STAT EG7+ Cartridge Abbott Point of Care, Princeton, NJ. The i-Stat EG7 cartridge is intended to be used for quantitatively measure sodium, potassium, ionized calcium, oxygen, carbon dioxide, partial pressure in arterial, venous, or capillary whole blood.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2131-2012·2012-08-08

    ICU Medical Flush Kits Recalled for Stopcock Molding Defect

    ICU Medical is recalling Flush Kits with 3 Way Off Stopcocks due to a molding defect that may occlude side ports.

    Product
    Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2135-2012·2012-08-08

    Stryker Recalls RF Cannulas Due to Packaging Error

    Stryker is recalling 226 units of RF Cannulas because 5mm and 10mm needles were incorrectly packaged in each other's boxes, posing a risk of thermal skin lesions.

    Product
    RF Cannula, 100 mm,Curved 10 MM, 20 G, REF 0406-630-125 RX only, Disposable ( 10/pk) Product Usage: The Stryker RF Cannulae, in combination with the Stryker RF Generator/Multi- Gen and electrodes, are intended for coagulation of soft tissue in orthopedic, arthroscopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2119-2012·2012-08-08

    Exactech Recalls Equinoxe Shoulder Arthroplasty Devices Due to Labeling Error

    Exactech is recalling Equinoxe shoulder arthroplasty devices because the labeling incorrectly states a ten-year shelf life, while the packaging is only qualified for five years.

    Product
    Equinoxe Reverse Glenosphere Locking Screw Intended for Primary and Reverse Total Shoulder Arthroplasty.
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-2120-2012·2012-08-08

    Exactech Recalls Orthopedic Devices Due to Incorrect Shelf Life Labeling

    Exactech is recalling specific orthopedic implants because the labeling incorrectly states a ten-year shelf life, while the packaging is only qualified for five years.

    Product
    Octane-C Cervical, 6¿ Lordotic Intended for anterior cervical spine intervertebral body fusion procedures at one level (C3-C7).
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-2110-2012·2012-08-08

    Beekley A-Spots Floral Skin Markers Recalled for Separation Defect

    Beekley Corporation is recalling 32,640 units of A-Spots Floral Skin Markers because the digital skin marker may separate from the backing material.

    Product
    Beekley A-Spots Floral Skin Markers -Order Number: 751 Product Usage: Mammography Skin Markers for marking: moles, scars, palpable masses or areas of concern
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2129-2012·2012-08-08

    ICU Medical Recalls Cardiac Catheterization Waste Management Systems

    ICU Medical is recalling Cardiac Catheterization Waste Management Systems due to a molding defect in a high pressure stopcock that could cause side ports to become occluded.

    Product
    Cardiac Catheterization Waste Management System w/1000mL Waste Bag, 2 Fluid Admin Sets Product Usage: For waste managment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2117-2012·2012-08-08

    Exactech Recalls Shoulder Arthroplasty Devices Due to Labeling Error

    Exactech is recalling Equinoxe shoulder arthroplasty devices because labeling incorrectly states a ten-year shelf life instead of the qualified five-year limit.

    Product
    Equinoxe Reverse Compression Screw Intended for Primary and Reverse Total Shoulder Arthroplasty.
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-2114-2012·2012-08-08

    Aesculap SIBD Trial Implants Recalled for Incorrect Part Number Etching

    Aesculap Implant Systems LLC is recalling 5 SIBD trial implants because the part numbers etched on the instruments may be incorrect, potentially causing selection errors.

    Product
    Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD 9 degree Trial Implant (SJ780T-US) Product Usage: The Aesculap Implant Systems SIBD Trial Implant instruments assist the surgeon in selecting the correct size implant for the patient
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2100-2012·2012-08-08

    Advanced Sterilization Products Recalls STERRAD Biological Indicators Due to Shelf-Life Data Gaps

    Advanced Sterilization Products is recalling specific lots of STERRAD CYCLESURE 24 Biological Indicators because the company lacks adequate data to support the product's full labeled shelf-life.

    Product
    STERRAD Cyclesure Biological Indicator (BI), P/N 14324 are sold in cases, packaged as part of STERRAD System Validation kits and STERRAD test packs. The STERRAD CYCLESURE 24 Biological Indicator (BI), P/N 14324 is intended to be used as a standard method for frequent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2109-2012·2012-08-08

    Beekley S-Spots Floral Skin Markers Recalled for Separation Defect

    Beekley Corporation is recalling 36,518 units of S-Spots Floral Skin Markers because the digital skin marker may separate from the backing material.

    Product
    Beekley S-Spots Floral Skin Markers -Order Number: 750 Product Usage: Mammography Skin Markers for marking: moles, scars, palpable masses or areas of concern
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2122-2012·2012-08-08

    Steris Reliance 130 Cart Washer Recall for Door Safety Feature Installation

    Steris is recalling 367 Reliance 130 and 130L Cart Washers to install a door close confirmation button and door open delay to ensure proper operation.

    Product
    The Reliance 130 and 130L Cart Washer/Disinfector is a high capacity mechanical washer intended for use in the washing, low-level disinfecting, and drying of carts, utensils, beds and other miscellaneous reusable items used in the care of patients at healthcare facilities…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2101-2012·2012-08-08

    Intuitive Surgical Recalls Instrument Arm Drapes Due to Adaptor Engagement Issues

    Intuitive Surgical is recalling specific lots of Instrument Arm Drapes because the sterile adaptor may have difficulty engaging an instrument during surgical procedures.

    Product
    INSTRUMENT ARM DRAPE IS2000, 20 PACK: Product Usage: The intended use of the Instrument arm drape is to protect equipment from contamination and to maintain a sterile field during surgical procedures using the da Vinci Surgical Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2103-2012·2012-08-08

    Intuitive Surgical Recalls Specific Lots of da Vinci Instrument Arm Drapes

    Intuitive Surgical is recalling specific lots of da Vinci Instrument Arm Drapes because the sterile adaptor may have difficulty engaging an instrument.

    Product
    KIT,DISPOSABLE ACCESSORY,4ARM,IS2000,5 PACK; Product Usage: The intended use of the Instrument arm drape is to protect equipment from contamination and to maintain a sterile field during surgical procedures using the da Vinci Surgical Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2111-2012·2012-08-08

    Beekley O-Spots Floral Skin Markers Recalled for Separation Defect

    Beekley Corporation is recalling 267,332 units of O-Spots Floral Skin Markers because the digital skin marker may separate from the backing material.

    Product
    Beekley O-Spots Floral Skin Markers -Order Number: 752 Product Usage: Mammography Skin Markers for marking: moles, scars, palpable masses or areas of concern
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2127-2012·2012-08-08

    GE OEC Medical Systems Recalls UroView 2800 Imaging Devices

    GE OEC Medical Systems is recalling UroView 2800 and other imaging devices due to hard disk drive issues. The recall covers 82 units distributed worldwide.

    Product
    UroView 2800; MDL number A349855. Product Usage: Designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical, and interventional procedures. Clinical application may include but are not limited to urologic and endoscopic procedures. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2116-2012·2012-08-08

    Exactech Recalls Equinoxe Shoulder Arthroplasty Devices Due to Labeling Error

    Exactech is recalling Equinoxe shoulder arthroplasty devices and related components because the labeling incorrectly states a ten-year shelf life instead of the qualified five-year shelf life.

    Product
    Equinoxe Fixed Angle Replicator Plate Intended for Primary and Reverse Total Shoulder Arthroplasty.
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-2118-2012·2012-08-08

    Exactech Recalls Shoulder and Spine Devices Due to Labeling Error

    Exactech is recalling Equinoxe and Octane-C devices because labeling incorrectly states a ten-year shelf life for parts qualified for five years.

    Product
    Equinoxe Reverse Shoulder Fracture Adapter Tray Screw Intended for Primary and Reverse Total Shoulder Arthroplasty.
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-2115-2012·2012-08-08

    Exactech Recalls Shoulder Arthroplasty Devices Due to Labeling Error

    Exactech is recalling Equinoxe shoulder arthroplasty devices because the labeling incorrectly states a ten-year shelf life instead of the qualified five-year shelf life.

    Product
    Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total Shoulder Arthroplasty
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-2112-2012·2012-08-08

    Beekley Altus Floral Skin Markers Recalled for Separation Defect

    Beekley Corporation is recalling 6,420 units of Altus Floral Skin Markers because the marker may separate from the backing material.

    Product
    Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: designed for Digital Mammography-Disposable skin markers for marking areas of concern or pain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2124-2012·2012-08-08

    Iris Diagnostics Recalls Urine Chemistry Control Material Due to Inaccurate Results

    Iris Diagnostics is recalling IRISpec CA/CB urine chemistry control material because nitrite results were incorrectly negative.

    Product
    IRISpec" CA/CB two-part urine chemistry control twin set, Iris Diagnostics part number 800-0074. Intended Use: IRISpec CA/CB is an assayed QC material for monitoring of the urine chemistry analytes and devices as listed on the package insert. For in vitro diagnostic (IVD)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2065-2012·2012-08-01

    GE OEC 8800 Flexview X-ray System Recalled for Safety Issues

    GE OEC Medical Systems is recalling OEC 8800 Flexview x-ray systems due to intermittent safety issues including navigation tracking inaccuracy and system lock-up.

    Product
    OEC 8800 Flexview, 892.1650 Image-intensified fluoroscopic x-ray system Product Usage: The 8800 Flexview is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical, and interventional procedures. Clinical applications may include…
    Category
    Medical Device
    Distribution
    Distributed nationwide