The Recall Desk

Hazard

Contamination recalls

2,096 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,096
Critical
84
Severe
838
Most recent
2026-10-21

Of the 2,096 contamination recalls we have scored against our rubric, 84 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 838 (40%) 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.

501–525 of 2096

  • HighFDA (Devices)·Z-0511-2023·2022-12-21

    Surgical Procedure Trays Recalled for Potential Sterile Barrier Compromise

    Stradis Medical is recalling 104 units of Henry Schein ENT surgical procedure trays due to incomplete sealing of the outer bag, which may compromise the sterility of the kit.

    Product
    HENRY SCHEIN, ENT PACK, Item No.570-2718
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0524-2023·2022-12-21

    Stradis Healthcare Surgical Knee Packs Recalled for Incomplete Sealing

    HENRY SCHEIN Knee Packs are being recalled due to incomplete outer bag sealing that may breach sterility. Affected surgical kits were distributed in the US and Canada.

    Product
    HENRY SCHEIN, Knee Pack, Item No.570-2908,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0525-2023·2022-12-21

    Stradis Healthcare catheter angiography kits recalled for defective sterile sealing

    Stradis Medical is recalling catheter angiography procedure kits with potentially incompletely sealed outer bags that may compromise the sterile integrity of the medical devices.

    Product
    HENRY SCHEIN, CATH ANGIO PACK, Item No.570-2930
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0478-2023·2022-12-21

    CarePoint 60 mL Syringes Recalled Due to Green Substance on Plunger

    Allison Medical recalls CarePoint 60 mL syringes due to green substance found on plungers. While the substance is nontoxic, its potential interaction with medications is unknown.

    Product
    CarePoint 60 mL Syringe Without Needle, REF: 04-7560
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Drugs)·D-0075-2023·2022-12-14

    Injectable Sodium Chloride Solution Recalled Due to Sterility Concerns and Leakage

    Fresenius Medical Care is recalling 0.9% Sodium Chloride Injection due to lack of sterility assurance from potential leakage. The nationwide recall affects injectable saline bags distributed in the United States.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0204-2023·2022-11-23

    CareFusion Sterilization Containers Fail Aerosol Challenge Testing

    CareFusion Genesis sterilization containers failed required aerosol challenge testing. The 1,143 affected units may not adequately sterilize surgical instruments.

    Product
    CareFusion V.Mueller GENESIS QTR-LENGTH CONTAINER 12 X 8" (30.3X20.3CM) 4" (10.2CM) DEEP STERRAD COMPATIBLE, REF CD0-4ST
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0067-2023·2022-11-23

    Adam's Polishes Hand Sanitizer Recalled for Methanol Contamination

    Adam's Polishes hand sanitizer with 75% isopropyl alcohol is being recalled due to methanol contamination found in certain lots manufactured under non-compliant conditions. The product was distributed nationwide.

    Product
    Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b) 8 fl. oz (237 mL) spray bottle, NDC 74943-125-08; c) 1 PINT / 16 fl. oz (475 ml.) spray bottle, NDC 74943-125-16; and d) 1 GALLON / 128 fl.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0178-2023·2022-11-16

    La Rosa Brand Pasteurized Crabmeat Recalled for Defective Seal

    RIVER CITY SEAFOOD INTERNATIONAL LLC is recalling 51 cases of La Rosa Brand BluCrab Pasteurized Crabmeat (lot #0531, best by 11/2023) due to defective seals that could allow contamination.

    Product
    La Rosa Brand BluCrab Pasteurized Crabmeat (Jumbo, Lump, Claw) Peso Neto: 454g Can label art is the same for all cans, there is a sticker for each category (Jumbo, Lump, Claw) that goes on the lid.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0109-2023·2022-11-09

    Joan of Arc Peppercorn Cheese Wheels Recalled for Listeria Contamination

    Old Europe Cheese is recalling Joan of Arc 2.2 lb peppercorn wheel cheese due to potential Listeria monocytogenes contamination. Affected products have best-by dates from September 28 to December 14, 2022.

    Product
    JOAN OF ARC 2.2 lb Joan of Arc Peppercorn Wheel no UPC
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·F-0110-2023·2022-11-09

    Reny Picot Brie Cheese Recall Due to Listeria Contamination Risk

    Old Europe Cheese is recalling Reny Picot and ST Randeaux double-crème Brie cheeses due to potential Listeria monocytogenes contamination. Affected products have best-by dates from September 28, 2022 to December 14, 2022.

    Product
    Reny Picot 6.5 lb Brie-dbl cr¿me w/Peppercorn, whole wheel no UPC; Reny Picot 8 oz Brie - dbl cr¿me w/Peppercorn, wedges, saran wrapped no UPC; ST RANDEAUX 8 oz Brie - dbl cr¿me w/Pepper, wedges, saran wrpd RW no UPC
    Category
    Food
    Distribution
    25 states
  • HighFDA (Drugs)·D-0051-2023·2022-11-09

    Prescription eye drops recalled due to sterility assurance defect

    Vital Care Compounder is recalling 378 droptainers of PRED ACETATE/GATIFLOXACIN eye drops distributed in AL, LA, MS, and TN due to inability to guarantee manufacturing sterility. No illnesses have been reported.

    Product
    PRED ACETATE / GATIFLOXACIN 1% / 0.5% SUSP, 10 mL droptainers, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-0027-2023·2022-11-09

    Acetylcysteine Eye Drops Recalled for Sterility Assurance Issues

    Acetylcysteine ophthalmic solution 5% from Vital Care Compounder is recalled due to manufacturing deficiencies that cannot ensure product sterility. The affected product was distributed in Alabama, Louisiana, Mississippi, and Tennessee.

    Product
    ACETYLCYSTEINE OPTH 5% Solution, 15 mL droptainers, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-0046-2023·2022-11-09

    Injectable Papaverine/Phentolamine Recalled Due to Sterility Assurance Failure

    Pharmacy Plus, Inc. is recalling 242 vials of papaverine/phentolamine injection because FDA inspection found the products were produced in conditions that cannot guarantee sterility. The affected lots were distributed to AL, LA, MS, and TN.

    Product
    PAPAVERINE / PHENTOLAMINE INJECTION 150MG / 5MG / VIAL SOLUTION, 10 mL vials, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Devices)·Z-0167-2023·2022-11-09

    NICU PICC Insertion Bundle Recalled for Breather Pouch Seal Defects

    Medline Industries recalls NICU PICC insertion bundles (50 kits) due to openings in breather pouch seals that compromise sterile barrier integrity. This Class II recall affects units distributed across the United States.

    Product
    CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O, REF CVI4470. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0162-2023·2022-11-09

    Medline Lithotomy Sterile Surgical Kit Recalled for Compromised Breather Pouch Seal

    Medline is recalling 96 sterile surgical kits (REF DYNJ50099C, Lot 22DBL482) distributed nationwide due to complaints of openings in breather pouches that compromise sterility and increase contamination risk.

    Product
    MEDLINE LITHOTOMY, REF DYNJ50099C. Convenience kit used in medical/surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0054-2023·2022-10-26

    Lyons Ready Care Thickened Apple Honey Nectar Recalled Due to Spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Apple Honey Nectar due to indications of product spoilage. The nationwide recall affects 645 cases with specific lot numbers and best-by dates in March 2023.

    Product
    Lyons Ready Care Thickened Apple Honey Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Food)·F-0053-2023·2022-10-26

    Lyons Ready Care Thickened Orange Nectar Recalled for Spoilage

    Lyons Magnus LLC is recalling Lyons Ready Care Thickened Orange Nectar due to indication of product spoilage. The recall affects 1,272 cases distributed nationwide with specific lot numbers and best-by dates in March 2023.

    Product
    Lyons Ready Care Thickened Orange Nectar packaged in combi-bloc multi wall paper cartons 46 fl oz cartons - 6 cartons to a case
    Category
    Food
    Distribution
    48 states
  • ModerateFDA (Food)·F-0037-2023·2022-10-19

    G-PREPROTEIN Liquid Dietary Supplement Recalled for Quality and Appearance Issues

    Novis PR, LLC recalled G-PREPROTEIN Liquid Dietary Supplement due to atypical bottle appearance, unusual odor, and atypical bubbles when opened. The recall affects 1,369 units distributed in Puerto Rico.

    Product
    G-PREPROTEIN, Liquid Predigested Protein, Dietary Supplement, Cherry Flavor, Net Contents 16 fl oz (473 mL), Kramer Novis
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0027-2023·2022-10-12

    Renaissance Food Group Recalls Veggie Kabobs Due to Listeria Contamination

    Renaissance Food Group is recalling 3 Skewer Veggie Kabobs due to confirmed Listeria monocytogenes contamination. Products were distributed in Alabama, Georgia, and South Carolina.

    Product
    3 Skewer Veggie Kabobs, NET WT, 1 LB 6 OZ (623g), Dist. By: Renaissance Food Group LLC 4322 Moreland Ave. Conley, GA 30288, UPC, ? 26766 19008 ?
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1822-2022·2022-10-05

    Humidifier Bottle and Syringe Filter Kit Sterile Barrier Breach Recall

    CooperSurgical is recalling BT37 benchtop incubator humidifier and filter kits due to a potential sterile barrier breach. The defect may allow unsterilized devices to contaminate and degrade embryos during incubation.

    Product
    Humidifier bottle and syringe filter kit (6 count of each) for the BT37 Mark I Benchtop Incubator (AY102295). The Mark I model is no longer produced, but the legacy humidifier bottle component design can also be used with the BT37 Mark II Benchtop Incubator.
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-1823-2022·2022-10-05

    CooperSurgical incubator humidifier kit recall due to sterile barrier breach

    CooperSurgical is recalling 5,182 humidifier bottle and filter kits for BT37 Mark II incubators due to potential sterile barrier damage from packaging defects. This could result in use of unsterilized components, risking embryo contamination.

    Product
    Humidifier bottle and syringe filter kit (6 count of each) for the BT37 Mark II Benchtop Incubator (AY200246)
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Food)·F-1776-2022·2022-09-28

    Blueberry Salsa Recalled Due to Inadequate Wash Water Sanitation

    Russ Davis Wholesale is recalling Blueberry Salsa due to inadequate sanitizer in wash water. The product was distributed to retailers in Iowa, Michigan, Minnesota, North Dakota, South Dakota, and Wisconsin.

    Product
    Blueberry Salsa. Contains: Mango, Blueberries, Red Bell Pepper, Pineapple, Green Bell Pepper, Papaya, Jalapeno Pepper, Onion, Orange, Cilantro, Lime Juice. Keep Refrigerated. Packaged in the following brands and sizes: 1. Item 85094. Net Wt. 8 oz. Crazy Fresh…
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1783-2022·2022-09-28

    Vegetable Medley from Russ Davis Wholesale Recalled for Inadequate Sanitizer

    Russ Davis Wholesale is recalling 87,915 units of Vegetable Medley products due to inadequate sanitizer in wash water. The recall affects products distributed across six Midwestern states.

    Product
    Vegetable Medley. Contains: Carrot, Broccoli, Cauliflower. Keep Refrigerated. Item 89334. Net Wt. 12 oz. Kowalski's Markets.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1767-2022·2022-09-28

    Veggie Tray with Ranch Dip Recalled Due to Inadequate Sanitizer

    Russ Davis Wholesale is recalling veggie trays sold under multiple brands due to inadequate sanitizer in wash water. Approximately 87,915 units were affected.

    Product
    Veggie Tray with Ranch Dip. Contains Baby Carrots, Cauliflower, Celery, Broccoli, and Ranch Dip. Keep Refrigerated. Item 80931. Net Wt. 3 lb. Packed under brands: Crazy Fresh, quick & easy, and grocery store branded.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1767-2022·2022-09-28

    Medical Device Recall: CARDIOHELP HLS Set Advanced Sterility Barrier Breach

    Maquet Medical Systems is expanding its recall of the CARDIOHELP HLS Set Advanced due to a potential breach in the sterility barrier that could compromise product sterility, affecting 6,871 US units and 18,670 worldwide.

    Product
    BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70106.9078. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide