The Recall Desk

Hazard

Contamination recalls

2,060 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,060
Critical
83
Severe
615
Most recent
2026-09-09

Of the 2,060 contamination recalls we have scored against our rubric, 83 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 615 (30%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all contamination recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1076–1100 of 2060

  • ModerateFDA (Devices)·Z-1402-2017·2017-03-15

    Metrex Recalls CaviWipes Extra Large Due to Packaging Contamination

    Metrex Research is recalling CaviWipes Extra Large surface disinfectants because they may have been contaminated during the packaging process.

    Product
    CaviWipes1 Extra Large, Part No. 13-5150 The brand name of the device is CaviWipes1 Extra Large, a surface disinfectant. The device has been assigned the product code LRJ (General Purpose Disinfectant) by the FDA and is classified as a Class I Medical Device. CaviWipes1 Extra La
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0496-2017·2017-03-08

    United Exchange Recalls Non-Sterile Eye Wash Bottles Nationwide

    United Exchange Corporation is recalling 46,080 bottles of Eye Wash due to direct evidence of non-sterility contamination in two lots.

    Product
    EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1479-2017·2017-03-01

    Wegmans Organic Dark Red Kidney Beans Recalled for Damaged Cans

    Hanover Foods is recalling Wegmans Organic Dark Red Kidney Beans because damaged cans could fracture and cause post-process contamination.

    Product
    Wegmans Organic Dark Red Kidney Beans, Net Wt. 15 OZ
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1466-2017·2017-02-15

    Blommer Recalls Cocie White Confectionery Discs Due to Salmonella Risk

    Blommer Chocolate Co. is recalling Cocie High Protein 90 White Confectionery Discs because the product contains milk and buttermilk powders that may be contaminated with Salmonella.

    Product
    Cocie High Protein 90 White Confectionery Discs - MB, NET WT: 40 LBS
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-0927-2017·2017-02-15

    Bayer Recalls Medrad Intego PET Infusion System Pumps

    Bayer is recalling Medrad Intego PET Infusion System pumps because the administration sets may produce particulates in radiopharmaceutical vials.

    Product
    MEDRAD Intego PET Infusion System - Pump Intended to deliver accurate doses of Fluoredeoxyglucose or F-Sodium Fluoride and commonly used flushing solutions to patients during molecular imaging (nuclear medicine) diagnostic procedures. It is also intended to provide effective rad
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1108-2017·2017-02-08

    PerkinElmer Spare Disk Remover Module Recall Due to Corrosion Risk

    PerkinElmer is recalling Spare Disk Remover Modules because defective axles may corrode in humid conditions, potentially contaminating test plates.

    Product
    Spare Disk Remover Module; Product Number: 61001820 Intended for in vitro quantitative and qualitative determination of analytes in body fluids.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1107-2017·2017-02-08

    PerkinElmer Genetic Screening Processor Recalled for Corroding Axles

    PerkinElmer is recalling 24 Genetic Screening Processor instruments because defective ball bushing axles may corrode in humid conditions, risking contamination of sample wells.

    Product
    Genetic Screening Processor (GSP); PerkinElmer Part Number= 2021-0010 Intended for in vitro quantitative and qualitative determination of analytes in body fluids.
    Category
    Medical Device
    Distribution
    4 states
  • CriticalFDA (Food)·F-1279-2017·2017-01-25

    American Instants Recalls Chai Tea Products Due to Salmonella Risk

    American Instants, Inc. is recalling various chai tea products, including Cappucino Supreme Gourmet Chai, because they may contain buttermilk and milk products contaminated with Salmonella.

    Product
    Cappucino Supreme Gourmet Chai Net Wt. 2 lbs.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1294-2017·2017-01-25

    Krasnyi Oktyabr Recalls Vobla Fish Due to Uneviscerated Product

    Krasnyi Oktyabr Inc. is recalling Vobla dry salted fish because FDA inspections found the product was uneviscerated. The product was distributed in New York and California.

    Product
    VOBLA - DRY EVISCERATED SALTED FISH, 5.29 oz. (150 g), UPC 4606495-001308 --- Product is vacuum packed and consists of salted dry caspian roach fish.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1231-2017·2017-01-25

    Steven Roberts Originals Recalls Dolcini for Potential Salmonella Contamination

    Steven Roberts Originals, LLC is recalling Dark Chocolate and Limoncello Dolcini because they were made with ingredients allegedly affected by a dry milk recall and potentially contaminated with Salmonella.

    Product
    Limoncello Dolcini , In clear plastic cup, 72 individual servings, Store frozen
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1011-2017·2017-01-18

    Symmetry Surgical ULTRA Sterrad Container Recall for Sealant Defect

    Symmetry Surgical is recalling 149 ULTRA Sterrad containers because deteriorated or missing base trim sealant may allow contaminants to enter the container after sterilization.

    Product
    symmetry surgical ULTRA(R) Sterrad container, REF numbers: C131310-SP, C13134-SP, C13135-SP, C13136-SP, C13139-SP, C13854-SP, C13855-SP, C13856-SP, C181310-SP, C18134-SP, C18135-SP, C18136-SP, C18138-SP, C22854-SP, C22855-SP, C22856-SP, C22858-SP, C24134-SP, C24135-SP, C24
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1010-2017·2017-01-18

    Symmetry Surgical ULTRA Steam Container Recall for Sealant Defect

    Symmetry Surgical is recalling ULTRA Steam containers because deteriorated or missing base trim sealant may allow contaminants to enter after sterilization.

    Product
    symmetry surgical ULTRA(R) Steam container, REF numbers: C131310, C13134, C13135, C13136, C13139, C13854, C13855, C13856, C181310, C18134, C18135, C18136, C18138, C22854, C22855, C22856, C22858, C24134, C24135, C24136 Product Usage: sterilization container
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1012-2017·2017-01-18

    Symmetry Surgical ULTRA Gravity Sterilizer Containers Recalled for Sealant Defect

    Symmetry Surgical is recalling 38 ULTRA Gravity sterilizer containers because deteriorated or missing base trim sealant could allow contaminants to enter the container.

    Product
    symmetry surgical ULTRA(R) Gravity container, REF numbers: C131310-G, C13134-G, C13135-G, C13136-G, C13139-G, C13854-G, C13855-G, C13856-G, C181310-G, C18134-G, C18135-G, C18136-G, C18138-G, C22854-G, C22855-G, C22856-G, C22858-G, C24134-G, C24135-G, C24136-G, C24138, C24138
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0928-2017·2017-01-04

    Sunset Natural Products Recalls HGH Dietary Supplement Capsules

    Sunset Natural Products Inc. is recalling HGH dietary supplement capsules pursuant to a consent decree requiring the destruction of products manufactured since April 2014.

    Product
    HGH, 100 capsules per bottle
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0914-2017·2017-01-04

    Sunset Natural Products Recalls Nutra Pro Dietary Supplements

    Sunset Natural Products Inc. is recalling Nutra Pro dietary supplements pursuant to a consent decree requiring the destruction of products manufactured since April 2014.

    Product
    Nutra Pro, 60 ct. per bottle
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0767-2017·2016-12-28

    Phil-Am Smoked Mackerel Recalled for Potential Botulism Contamination

    Phil-Am Trading is recalling smoked mackerel due to potential Clostridium botulinum contamination, which can cause life-threatening illness.

    Product
    Phil-Am Smoked Mackerel (Hasa Hasa) Net. Wt. 200g (7.05 oz.) packaged: Clear flexible plastic pouch and is topped by a predominantly red tag affixed to the top seal which has the products information.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0762-2017·2016-12-28

    Naturecom Recalls DMAA Powder Due to Potential Presence of 1,3-Dimethylamylamine

    Naturecom is recalling 500g bags of DMAA powder because the product may contain 1,3-dimethylamylamine. The recall covers products distributed nationwide and internationally.

    Product
    DMAA (1,3-Dimethylamylamine) Net Weight 500g Product is packaged in approximately 8" x 11 silver and clear mylar ziplock bags that contain 500g of DMAA.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0231-2017·2016-12-28

    Sage Products Recalls Chlorhexidine Gluconate Cloth Due to CGMP Deviations

    Sage Products LLC is recalling 2% Chlorhexidine Gluconate Cloth due to CGMP deviations and potential contamination. The product was distributed nationwide and internationally.

    Product
    CHLORHEXIDINE GLUCONATE — CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE GLUCONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0727-2017·2016-12-14

    AMD-Ritmed Transparent Dressing Recalled for Sterility Failure

    AMD-Ritmed is recalling Lot 68408 of transparent dressings because FDA testing found the sterile products were contaminated.

    Product
    AMD-Ritmed Transparent Dressing - Window with label, 4 " x 4 3/4" (10 cm x 12 cm), Reorder No./Code A60044-W, Sterile -- 200 Dressings per case -- Made in China for AMD-Ritmed Inc. 1200 55th Ave., Lachine, QC H8T 3J8/295 Firetower Road, Tonawanda, NY 14150
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Food)·F-0676-2017·2016-12-14

    Airheads Mini Bars Recalled Due to Blood Observed on Packaging Equipment

    Perfetti Van Melle USA Inc is recalling Airheads Mini Bars because blood was observed on packaging equipment. The recall covers 4,147 cases distributed nationwide.

    Product
    Airheads Mini Bars 12oz bags of assorted flavors. 12 - 12oz bags are included in cardboard cartons. Assorted flavors include Cherry, Watermelon, Blue Raspberry, and White Mystery.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0553-2017·2016-12-07

    Island Soups Red Peas Soup Recalled for Botulism Risk

    Island Soups Company Inc. is recalling Red Peas Soup due to possible contamination with Clostridium botulinum. Consumers should check their pantry for affected cans.

    Product
    ISLAND SOUPS, RED PEAS SOUP, NET WT. 16 OZ (28.4G)
    Category
    Food
    Distribution
    Distributed nationwide