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

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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

24326–24350 of 40175

  • HighFDA (Devices)·Z-1222-2018·2018-04-04

    Inova Diagnostics Recalls QUANTA-Lyser 240 EIA Due to Power Supply Defect

    Inova Diagnostics is recalling one QUANTA-Lyser 240 EIA instrument because a defective power supply may cause loss of protective grounding.

    Product
    QUANTA-Lyser 240 EIA, Part #GS0241. The instrument is a fully automated, high-throughput, bench top system designed for clinical use to automate slide and reagent barcode reading, sample dilution and distribution, reagent pipetting and dispensing, slide and plate washing…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1185-2018·2018-04-04

    Cook Inc. Recalls IVF Embryo Transfer Syringes Due to Quality Testing Gaps

    Cook Inc. is recalling specific lots of Norm-Ject Tuberkulin Syringes used for IVF embryo transfer because they were distributed without completed quality testing.

    Product
    Norm-Ject Tuberkulin Syringe, Catalog Number: K-ATS-1000, Global Product Number: G19871 Product Usage: Used to place in vitro fertilized (IVF) embryos into the uterine cavity. Intended for one-time use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1196-2018·2018-04-04

    Zimmer Biomet Recalls AIM Tibial Nails Due to High Revision Rates

    Zimmer Biomet is recalling AIM Tibial Nails because the surgical revision rate exceeded acceptance criteria in a clinical analysis.

    Product
    AIM Tibial Nails intramedullary fixation rod - STERILE; Item numbers: 800508255 NAIL TIB DYN 08X25.5 - STERILE 800508270 NAIL TIB DYN 08X27.0 - STERILE 800508285 NAIL TIB DYN 08X28.5 - STERILE 800508300 NAIL TIB DYN 08X30.0 - STERILE 800508315 NAIL TIB DYN 08X31.5 - STERILE…
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1182-2018·2018-04-04

    Madison Polymeric Engineering Recalls First Step Flexible Endoscope Bedside Pre-Clean Kit

    Madison Polymeric Engineering is recalling 285 cases of the First Step Flexible Endoscope Bedside Pre-Clean Kit because affected lots may have exceeded microbial limits.

    Product
    First Step Flexible Endoscope Bedside Pre-Clean Kit, EP-4. Intended for pre-clean of outer surface of flexible scopes and surgical instruments to remove gross contamination prior to manual cleaning and disinfection. Product Labeling: "The multi-tiered enzymatic detergent starts…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1213-2018·2018-04-04

    Konica Minolta Sonimage HS1 Ultrasound Kit AC Adapter Recall

    Konica Minolta is recalling 85 Sonimage HS1 Ultrasound Kit AC adapters due to a risk of circuit board breakage and smoke emission.

    Product
    Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8WA, UDI: 04560141944534
    Category
    Medical Device
    Distribution
    35 states
  • ModerateFDA (Devices)·Z-1273-2018·2018-04-04

    Mesa Laboratories Recalls ProSpore Biological Indicators Due to Concentration Defect

    Mesa Laboratories is recalling specific lots of ProSpore Biological Indicators because the concentration of bromocresol purple does not conform to specification.

    Product
    ProSpore Biological Indicator Part Numbers: PS-6-50, PS-5-50, PS-4-10, PS-4-50, 3471
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1202-2018·2018-04-04

    Johnson & Johnson Recalls COACH Self-Adhering Sports Wraps for Latex Labeling Error

    Johnson & Johnson is recalling COACH Self-Adhering Sports Wraps because the label incorrectly states they are not made with natural rubber latex, though latex was used in early manufacturing.

    Product
    COACH¿ Self-Adhering Sports Wrap (size: 3in)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1203-2018·2018-04-04

    Johnson & Johnson Recalls First Aid Wraps Due to Latex Labeling Error

    Johnson & Johnson is recalling select first aid wraps because they were labeled as latex-free but used natural latex in early manufacturing.

    Product
    Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 2in)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1193-2018·2018-04-04

    Teleflex Visistat 35 Skin Closure Devices Recalled for Labeling Error

    Teleflex Medical is recalling Visistat 35 skin closure devices because some boxes are mislabeled as Wide when they contain Regular devices.

    Product
    Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1183-2018·2018-04-04

    Quidel Recalls Sofia 2 Analyzers Due to Calibration Error

    Quidel is recalling 482 Sofia 2 Analyzers because a manufacturing error may cause calibration failure or incorrect test results.

    Product
    Sofia 2 Analyzer Catalog Number 20299 Sofia 2 is a bench top analyzer intended to be used with Cassette-based immunofluorescent in vitro diagnostic assays . Sofia 2 is intended for professional and laboratory use.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1238-2018·2018-04-04

    Zimmer Biomet Recalls Partial Knee Spacer Block Instruments

    Zimmer Biomet is recalling specific Persona Partial Knee spacer block instruments because they do not fit in the alignment tower instrument or handle.

    Product
    Persona Partial Knee spacer block instruments; (1) 8mm block, Model Number: 42-5399-035-08; (2) 9mm block, Model Number:42-5399-035-09; (3) 10mm block, Model Number: 42-5399-035-10; (4) 12mm block, Model Number: 42-5399-035-12; (5) 14mm block, Model Number: 42-5399-035-14 A…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1269-2018·2018-04-04

    Roche Modular E 170 Analyzer Recalled for Questionable Results

    Roche Diagnostics is recalling Modular E 170 Analyzers because using 13 mm sample tubes without adapters may cause questionable test results.

    Product
    Modular E 170 Analyzer: Immunoassay Chemistry Analyzer, Chemistry (Photometric, Discrete) for clinical use, Catalog Numbers: 03739040692, 03023109001, 05023599001, 05023572001, 03739040001 & 03023109973.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1190-2018·2018-04-04

    Zimmer Dental Recalls Tapered Screw-Vent Implants Due to Mislabeled Lots

    Zimmer Dental Inc is recalling Tapered Screw-Vent MTX dental implants because two lots with different thread diameters were commingled and may be mislabeled.

    Product
    Tapered Screw-Vent MTX, Dental Implant, sterile. Model TSV4B10.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1239-2018·2018-04-04

    Zimmer Biomet Recalls Coonrad/Morrey Elbow Implant Humeral Assemblies

    Zimmer Biomet is recalling nine Coonrad/Morrey Elbow Implant humeral assemblies because they are missing required humeral bushing components.

    Product
    Coonrad/Morrey Elbow Implant System humeral assembly 4IN XSML, Item Number: 32-8105-027-04 (UDI: (01)0088902427 4006(17)220731(10)63694912)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1204-2018·2018-04-04

    Johnson & Johnson Recalls Select First Aid Wraps Due to Latex Labeling Error

    Johnson & Johnson is voluntarily recalling select first aid wraps because the label incorrectly states they are not made with natural rubber latex.

    Product
    Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 3in)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1205-2018·2018-04-04

    Johnson & Johnson Recalls First Aid Wraps Due to Latex Labeling Error

    Johnson & Johnson is voluntarily recalling select first aid wraps because the 'not made with natural rubber latex' label is inaccurate.

    Product
    Johnson & Johnson BAND-AID¿ Brand First Aid Products HURT-FREE¿ Wrap (size: 1in)
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1199-2018·2018-04-04

    GE Healthcare Recalls Datex-Ohmeda Anesthetic Cassettes for Quality Control Issues

    GE Healthcare is recalling two Datex-Ohmeda AISYS CS2 Aladin2 cassettes because they were shipped without proper evaluation and may be nonconforming.

    Product
    DATEX-OHMEDA AISYS CS2 ALADIN2 CASSETTE Cassettes are intended to be used to deliver anesthetic agent.
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1173-2018·2018-04-04

    Biomet Recalls Orthopedic Implants Due to Screw Hole Mismatch

    Biomet is recalling 634 Zimmer Biomet Comprehensive Segmental Revision System implants because a screw hole mismatch may prevent proper assembly during surgery.

    Product
    Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic implants for Proximal Humeral Reconstruction, Distal Humeral Reconstruction, and Total Humeral Reconstruction
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1209-2018·2018-04-04

    Johnson & Johnson Recalls ACUVUE OASYS Contact Lenses Due to Foreign Matter

    Johnson & Johnson Vision Care is recalling specific lots of ACUVUE OASYS contact lenses because foreign matter was found between the blister package and foil.

    Product
    ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1211-2018·2018-04-04

    Johnson & Johnson Recalls 1-DAY ACUVUE Moist for Astigmatism Contact Lenses

    Johnson & Johnson Vision Care is recalling 1-DAY ACUVUE Moist for Astigmatism contact lenses due to reports of foreign matter found between the blister package and foil.

    Product
    1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1271-2018·2018-04-04

    MedComp Recalls CT Port Kits Packaged with Incorrect Unmarked Guidewire

    Medical Components, Inc. is recalling 8F Plastic Dignity Low Profile CT Port kits because they were packaged with unmarked guidewires instead of the marked ones indicated on the label.

    Product
    8F Plastic Dignity¿ Low Profile CT Port W/Pre-Attached ChronoFlex¿ Polyurethane Catheter
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1241-2018·2018-04-04

    Encore Medical Recalls AltiVate Reverse Humeral Socket Shell Trials

    Encore Medical is recalling AltiVate Reverse Humeral Socket Shell Trials due to broken or missing screws and retaining clips.

    Product
    AltiVate Reverse INSTRUMENTATION, HUMERAL SOCKET SHELL TRIAL, STANDARD, REF 804-06-152, Qty: 01, Encore Medical, LP Orthopedic surgical instrument. Product Usage: The humeral socket shell trial is used to replicate/trial the shell geometry of the AltiVate Reverse Standard…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1172-2018·2018-04-04

    Getinge Hemashield Cardiovascular Fabric Recalled for Packaging Mislabeling

    Getinge US Sales LLC is recalling Hemashield Knitted Double Velour Cardiovascular Fabric because the packaging label lists a different product size than the actual item inside.

    Product
    HEMASHIELD Knitted Double Velour Cardiovascular Fabric
    Category
    Medical Device
    Distribution
    1 state