The Recall Desk

Hazard

Product Contamination recalls

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

What the numbers show

Total
28
Critical
5
Severe
10
Most recent
2026-05-13

Of the 28 product contamination recalls we have scored against our rubric, 5 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 10 (36%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all product 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.

1–25 of 28

  • SevereFDA (Drugs)·D-0518-2026·2026-05-13

    BD PurPrep Povidone-Iodine Topical Solution Sterility Assurance Recall

    CareFusion 213, LLC is recalling BD PurPrep (povidone-iodine 8.3% with isopropyl alcohol 72.5%) due to lack of assurance of sterility and potential product contamination. Affected lots are distributed nationwide.

    Product
    PURPREP — PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0237-2024·2024-01-24

    Ibuprofen and Famotidine Tablets Recalled for Foreign Tablet Contamination

    Ascend Laboratories is recalling 3,288 bottles of Ibuprofen and Famotidine tablets nationwide because a stray Rasagiline Mesylate tablet was discovered in an unopened bottle during quality control.

    Product
    IBUPROFEN AND FAMOTIDINE — IBUPROFEN AND FAMOTIDINE (IBUPROFEN AND FAMOTIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0223-2024·2024-01-17

    Tizanidine 4mg Tablets Recalled for Contamination with 2mg Tablets

    Dr. Reddy's Laboratories is recalling Tizanidine 4mg tablets due to the presence of 2mg tablets in bottles. About 38,952 bottles were distributed nationwide.

    Product
    TIZANIDINE — TIZANIDINE (TIZANIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0205-2024·2024-01-03

    Sertraline Hydrochloride Tablets Recalled Due to Manufacturing Process Defect

    Legacy Pharmaceutical Packaging LLC is recalling 161,664 bottles of Sertraline Hydrochloride 100 mg tablets distributed in California and Arkansas due to inadequate line clearance during manufacturing that may result in product comingling.

    Product
    SERTRALINE HYDROCHLORIDE — SERTRALINE HYDROCHLORIDE (SERTRALINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0049-2024·2023-10-25

    Betaxolol Hydrochloride tablets recalled due to oxycodone contamination

    KVK-Tech's Betaxolol Hydrochloride tablets (10 mg, lot 17853A) are being recalled nationwide due to potential contamination with oxycodone tablets. Patients should stop using affected bottles immediately and contact their healthcare provider.

    Product
    BETAXOLOL HYDROCHLORIDE — BETAXOLOL HYDROCHLORIDE (BETAXOLOL HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0570-2023·2023-05-17

    Gabapentin tablets recalled due to product mixup with foreign tablet

    The Harvard Drug Group recalled 3,984 cartons of Gabapentin 600 mg tablets distributed nationwide due to a product mixup where one foreign tablet was found.

    Product
    GABAPENTIN — GABAPENTIN (GABAPENTIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1044-2023·2023-02-08

    Biopsy Medium for In Vitro Fertilization Recalled Due to Product Contamination

    CooperSurgical is recalling a lot of Biopsy Medium used in IVF procedures because the product may contain an incorrect medium that could degrade embryos. No illnesses have been reported.

    Product
    BIOPSY MEDIUM 10ML, Reference Number 10620010 A, used for blastomere biopsy of cleavage stage embryos for Pre-implantation Genetic Diagnosis (PGD)
    Category
    Medical Device
    Distribution
    0 states
  • SevereUSDA FSIS·028-2022·2022-08-30

    Connoisseur’s Kitchen Recalls Imported Frozen Chicken Entrees Over Listeria Risk

    Connoisseur’s Kitchen is recalling approximately 880 pounds of imported frozen ready-to-eat chicken entrees due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    Connoisseur’s Kitchen Recalls Imported Frozen Chicken Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0399-2022·2021-12-29

    Cholesterol Reagent Recalled for Calibration Failures and Erroneous Results

    Beckman Coulter is recalling 1,433 units of a cholesterol reagent that may fail calibration and produce erroneous low test results. Affected units were distributed nationwide and internationally.

    Product
    SYNCHRON Systems Cholesterol (CHOL) Reagent, REF: 467825
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0722-2021·2021-08-18

    Cimetidine Hydrochloride Oral Solution Recalled for CGMP Violation

    Pharmaceutical Associates Inc. is recalling Cimetidine Hydrochloride Oral Solution 300 mg/5 mL due to a lack of Current Good Manufacturing Practice (CGMP) and potential carryover of Senna Syrup.

    Product
    Cimetidine Hydrochloride Oral Solution 300 mg/5 mL, 8 fl oz (237 mL) Rx ONLY, Pharmaceutical Associates, Inc. Greenville, SC 29605, NDC 0121-0649-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·026-2021·2021-07-29

    Greater Omaha Packing Recalls Raw Beef Products for E. Coli O157:H7

    Greater Omaha Packing is recalling approximately 295,236 pounds of raw beef products intended for non-intact use due to possible E. coli O157:H7 contamination.

    Product
    Greater Omaha Packing Co., Inc. — Greater Omaha Packing Recalls Raw Beef Products Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    4 states
  • HighFDA (Drugs)·D-0602-2021·2021-06-09

    Buspirone Hydrochloride Tablets Recalled for Foreign Tablet Contamination

    Oxford Pharmaceuticals is recalling 6,864 bottles of Buspirone Hydrochloride Tablets, 15 mg, distributed nationwide due to the presence of foreign tablets or capsules in the product.

    Product
    BUSPIRONE HYDROCHLORIDE — BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-02022021-01·2021-02-02

    Raw Ground Beef Alert: Possible E. Coli O157:H7 Contamination

    USDA FSIS issued a public health alert for raw ground beef sold in Sandwich, Illinois, due to possible E. coli O157:H7 contamination. Consumers should discard or return the product.

    Product
    FSIS Issues Public Health Alert for Raw Ground Beef Product Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    1 state
  • CriticalUSDA FSIS·012-2020·2020-06-13

    Lakeside Refrigerated Services Recalls Ground Beef Due to E. coli O157:H7 Risk

    Lakeside Refrigerated Services is recalling approximately 42,922 pounds of ground beef products that may be contaminated with E. coli O157:H7.

    Product
    Lakeside Refrigerated Services — Lakeside Refrigerated Services Recalls Beef Products due to Possible E.coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·076-2019·2019-07-20

    US Foods Recalls Raw Beef and Pork Due to Possible Contamination

    US Foods is recalling approximately 712 pounds of raw beef and pork products that may be contaminated due to a potential employee injury during production.

    Product
    US Foods Inc. — US Foods Recalls Raw Beef and Pork Products Due to Possible Product Contamination
    Category
    Food
    Distribution
    6 states
  • HighUSDA FSIS·pha-07202018-1·2018-07-20

    FSIS Public Health Alert for Hungry Man Dinners with Recalled Whey Powder

    The USDA FSIS issued a public health alert for Hungry Man frozen dinners containing whey powder recalled due to possible Salmonella contamination. No adverse reactions have been reported.

    Product
    FSIS Issues Public Health Alert For Products Containing FDA-Regulated Whey Powder That Has Been Recalled Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·033-2018·2018-04-14

    Fresh Foods Manufacturing Recalls Ready-to-Eat Salads Due to E. coli O157:H7

    Fresh Foods Manufacturing Co. is voluntarily recalling approximately 8,757 pounds of ready-to-eat salad products due to possible E. coli O157:H7 contamination.

    Product
    Fresh Food Manufacturing Company — Fresh Foods Manufacturing Co. Recalls Ready-To-Eat Salad Products Due to Possible E. coli O157:H7 Contamination
    Category
    Food
    Distribution
    5 states
  • HighUSDA FSIS·pha-112017·2017-11-20

    USDA Alerts on Poultry Products Lacking Import Inspection

    USDA FSIS issued a public health alert for approximately 6,907 pounds of chicken products that were not presented for re-inspection after containing recalled ingredients.

    Product
    Productos Dany Inc. — FSIS Issues Public Health Alert for Poultry Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·031-2016·2016-04-21

    Meating Place Recalls Beef Patties Due to Possible E. Coli O157:H7 Contamination

    Meating Place is recalling approximately 325 pounds of ground beef patties that may be contaminated with E. coli O157:H7. The product was shipped to retail and institutional locations in the Buffalo, NY area.

    Product
    Meating Place Lorigo's Meating Place Inc. — Meating Place Recalls Beef Product Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·141-2015·2015-11-17

    Tyson Recalls Fully Cooked Hot Wings Due To Off Odor

    Tyson Foods is recalling approximately 52,486 pounds of fully cooked hot wings due to possible adulteration from an off odor.

    Product
    Tyson Foods, Inc. — Tyson Foods Inc. Recalls Chicken Product Due To Possible Adulteration
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·130-2015·2015-10-22

    Rustico Foods Recalls Packaged Soup Products Produced Without Federal Inspection

    Rustico Foods is recalling approximately 2,659 pounds of packaged soup products produced without the benefit of federal inspection. The products were shipped to retail establishments in southern California.

    Product
    Rustico Foods Recalls Packaged Soup Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·070-2015·2015-04-27

    Skyline Provisions Recalls Beef Products Due To E. Coli O157:H7 Contamination

    Skyline Provisions is recalling 1,029 pounds of beef products contaminated with E. coli O157:H7. The recall was announced by the USDA Food Safety and Inspection Service.

    Product
    Skyline Provisions — Skyline Provisions, Inc., Recalls Beef Products Due To E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·061-2014·2014-09-25

    Caviness Beef Packers Recalls Beef Trimmings Due To E. Coli O157:H7

    Caviness Beef Packers is recalling approximately 23,100 pounds of beef trimmings produced in August 2014 due to possible E. coli O157:H7 contamination.

    Product
    Caviness Beef Packers, Ltd. — Texas Firm Recalls Beef Products Due To Possible E. Coli O157:H7
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-2486-2014·2014-09-10

    Customed Recalls Surgical Packs Due to Potential Packaging Integrity Issues

    Customed, Inc. is recalling specific lots of EO-sterilized surgical packs because packaging integrity may be compromised, potentially leading to product contamination or loss of sterility.

    Product
    Shoulder pack (I) (2), code 900-2515 (1) GOWN IMP. XTRA REINF. XL TOWEL WRAP LEVEL Ill (1) TOWEL ABSORBENT 15" X 20" (1) GOWN XXL SMS IMPERVIOUS REINFORCED (1) MAYO STAND COVER REINFORCED (2) STRIPS TAPE 24" X 4" (1) SUTURE BAG FLORAL (1) SHEET SPLIT W/ADHESIVE 1 08" X 77"
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2529-2014·2014-09-10

    Customed Recalls EO Sterilized Surgical Gowns Due to Packaging Integrity Concerns

    Customed, Inc. is recalling EO sterilized surgical gowns because packaging integrity may be compromised, potentially leading to product contamination or loss of sterility.

    Product
    Gown Impervious , Code 900-3190, contains: GOWN IMPERVIOUS EXTRA LONG X-LARGE WITH TOWEL & WRAP Product Usage: EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.
    Category
    Medical Device
    Distribution
    Distributed nationwide