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.

Filters

Agency

All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

23401–23425 of 40299

  • ModerateFDA (Devices)·Z-2268-2018·2018-06-27

    Smith & Nephew Recalls Birmingham Hip Resurfacing Acetabular Cups for Labeling Defects

    Smith & Nephew is recalling six Birmingham Hip Resurfacing Acetabular Cups because they were distributed in the US with international labeling instead of FDA-approved instructions.

    Product
    Birmingham Hip Resurfacing Acetabular Cup with Impactor: (a) Size 56 mm, REF 74120156 (b) Size 64 mm, REF 74120164 (c) Size 54 mm, REF 74122154 (d) Size 58 mm, REF 74122158 (e) Size 60 mm, REF 74122160 (f) Size 62 mm, REF 74122162
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Devices)·Z-2257-2018·2018-06-27

    Quantimetrix Recalls Dropper Plus Urinalysis Control Kits Due to Lot Error

    Quantimetrix Corporation is recalling 20 kits of Dropper Plus Point-of-Care Urinalysis Dipstick Control because they contained an incorrect lot of Level 1 vials.

    Product
    Dropper Plus Point-of-Care Urinalysis Dipstick Control kit The Quantimetrix Dropper Plus Point-of-Care Urinalysis Dipstick Control is intended as a control for urinalysis reagent strips, microalbumin, and creatinine by the listed test methods, and as a control for…
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2156-2018·2018-06-20

    Sun Med Recalls Adult Manual Resuscitators Due to Port Detachment Risk

    Sun Med, LLC is recalling 361 cases of Medline Adult Manual Resuscitators because the patient port retaining ring may not fully seat, potentially allowing the port to detach and impacting air delivery.

    Product
    MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, FILTER, PEEP VALVE AND 7 FT. OXYGEN TUBING, REF CPRM1126FP
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2212-2018·2018-06-20

    Angiodynamics Recalls RS Tandem 5F DL Xcela PICC Catheters

    Angiodynamics Inc. is recalling 13 boxes of RS Tandem 5F DL Xcela PICC catheters because a component may contain unsafe levels of bacterial endotoxins.

    Product
    RS TANDEM 5F DL XCELA PICC PASV, Catalog Number 60M181582
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2217-2018·2018-06-20

    Angiodynamics Recalls PICC Nursing Trays Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling 2 boxes of CAN 5F DL BIOFLO PASV PICC Nursing Trays because a component may contain unsafe levels of bacterial endotoxins.

    Product
    CAN 5F DL BIOFLO PASV PICC NURSING TRAY, Catalog Number 60M700936
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2210-2018·2018-06-20

    Angiodynamics Recalls 5F DL BIOFLO PICC Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 5F DL BIOFLO PICC kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    5F DL BIOFLO PICC, Catalog Number 60M180592
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2175-2018·2018-06-20

    Philips Brilliance 16 CT System Recalled for Head Holder Contact Hazard

    Philips is recalling two Brilliance 16 CT systems because the patient support head holder may contact the back ISO shelter wall, posing a risk of serious injury.

    Product
    Brilliance 16 with DEPMED HARDENING KIT 12NC: 453567400741, Model Number 728240. Computed Tomography X-ray system
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2218-2018·2018-06-20

    Angiodynamics Recalls XCELA PICC Kits Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling 17 boxes of CAN 5F SINGLE XCELA PICC kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    CAN 5F SINGLE XCELA PICC, Catalog Number 60M701531
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2202-2018·2018-06-20

    Angiodynamics Recalls Bioflo Midline Catheters Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling 3 boxes of RS - TANDEM 5F DL BIOFLO MIDLINE catheters because a component may contain unsafe levels of bacterial endotoxins.

    Product
    RS - TANDEM 5F DL BIOFLO MIDLINE, Catalog Number 60M035472
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2196-2018·2018-06-20

    Angiodynamics Recalls Bio-Stable Kits Due to Bacterial Endotoxin Risk

    Angiodynamics Inc. is recalling 298 boxes of Bio-Stable 5F kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved with Nitinol Guidewire PG, Catalog Number 45-895
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2176-2018·2018-06-20

    Philips Brilliance 16 P CT Systems Recalled for Head Holder Contact Risk

    Philips is recalling 20 Brilliance 16 P CT systems because the patient support head holder may contact the back ISO shelter wall, posing a risk of serious injury.

    Product
    Brilliance 16 P with DEPMED HARDENING KIT 12NC: 453567400741, Model Number 728246. Computed Tomography X-ray system
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2153-2018·2018-06-20

    Sun Med Recalls Adult Manual Resuscitators Due to Port Detachment Risk

    Sun Med, LLC is recalling 113 cases of Medline Adult Manual Resuscitators because the patient port retaining ring may not fully seat, potentially allowing the port to detach during use.

    Product
    MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, CO2 AND 7 FT. OXYGEN TUBING, REF CPRM1126C
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2192-2018·2018-06-20

    Angiodynamics Recalls Bio-Stable Kits Due to Bacterial Endotoxin Risk

    Angiodynamics Inc. is recalling 17 boxes of Bio-Stable 5F kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    Bio-Stable 5F SL-55CM IR-145 Kit Valved with Nitinol GW PG, Catalog Number 45-882
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2228-2018·2018-06-20

    Seaberg SAM XT-C Tourniquet Recalled for Potential Buckle Stitch Failure

    The Seaberg Company is recalling SAM XT-C tourniquets because internal testing showed stitches securing the buckle could fail, posing a risk of serious injury or death.

    Product
    Part #: SAM XT-C, Model: Hi-Viz Blue
    Category
    Medical Device
    Distribution
    23 states
  • SevereFDA (Devices)·Z-2223-2018·2018-06-20

    Angiodynamics Recalls BioFlo PICC Kits Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling BioFlo PICC nursing kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    BioFlo PICC (NV) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol Wire PG, Catalog Number 75-033
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2213-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL XPP Kits Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling 5 boxes of RS 5F DL XPP Kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL XPP KIT, Catalog Number 60M183104
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2214-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL BIOFLO PASV Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 104 boxes of RS 5F DL BIOFLO PASV kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL BIOFLO PASV, Catalog Number 60M183481
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2205-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL BIOFLO PASV Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 2 boxes of RS 5F DL BIOFLO PASV kits because components may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL BIOFLO PASV, Catalog Number 60M132324
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2222-2018·2018-06-20

    BioFlo PICC Nursing Kit Recalled for Unsafe Bacterial Endotoxin Levels

    Angiodynamics Inc. is recalling BioFlo PICC Nursing Kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    BioFlo PICC (NV) 5FSL-55cm Maximal Barrier Nursing Kit w/ 70cm Nitinol Wire PG, Catalog Number 75-032
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2152-2018·2018-06-20

    Sun Med Recalls Adult Manual Resuscitators Due to Port Detachment Risk

    Sun Med, LLC is recalling 350 cases of Medline Adult Manual Resuscitators because the patient port retaining ring may not fully seat, potentially allowing the port to detach during use and impacting air delivery.

    Product
    MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR AND 7 FT. OXYGEN TUBING, REF CPRM1126
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2174-2018·2018-06-20

    Philips Brilliance 64 CT System Recalled for Patient Support Head Holder Hazard

    Philips is recalling three Brilliance 64 CT systems because the patient support head holder could contact the back ISO shelter wall, posing a risk of serious injury.

    Product
    Brilliance 64 with DEPMED HARDENING KIT 12NC: 459800191351, Model Number 728231. Computed Tomography X-ray system
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2226-2018·2018-06-20

    Seaberg SAM XT-M Tourniquet Recalled for Potential Buckle Failure

    The Seaberg Company is recalling SAM XT-M tourniquets because internal testing found stitches securing the buckle could fail, posing a risk of serious injury or death.

    Product
    Part #: SAM XT-M, Model: Tactical Black or Military
    Category
    Medical Device
    Distribution
    23 states