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.

1876–1900 of 2060

  • ModerateFDA (Devices)·Z-1315-2013·2013-05-22

    Karl Storz Cutting Electrodes Recalled for Packaging Damage

    Karl Storz is recalling 9,432 cutting electrodes due to possible damage to sterile packaging that may allow airborne contamination.

    Product
    Electrode, Cutting, 24FR, 0.30MM (27040G-.30/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1308-2013·2013-05-22

    Karl Storz Recalls Sterile Electrodes Due to Packaging Damage

    Karl Storz is recalling 9,432 sterile ball-end electrodes because damaged packaging may allow airborne contamination.

    Product
    Electrode, Coag, Ball End, 24FR (27050N/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-316-2013·2013-05-15

    Hospira Recalls Sodium Acetate Injection Due to Sterility Concerns

    Hospira Inc. is recalling 266,900 vials of Sodium Acetate Injection due to loose crimps that may compromise sterility.

    Product
    SODIUM ACETATE — SODIUM ACETATE (SODIUM ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1269-2013·2013-05-15

    Baxter Recalls Non-DEHP Y-Type Catheter Extension Sets Due to Sterility Compromise

    Baxter Healthcare is recalling 228,200 units of Non-DEHP Y-Type Catheter Extension Sets because separating packages can compromise the sterile barrier of adjacent units.

    Product
    A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set, 5.7", Vol. 0.8 mL, 2 Injection Sites, Male Luer Lock Adapter, Single use only Product Usage: This device is indicated for use in blood sampling and the administration of solutions. The InterLink Injection S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-276-2013·2013-05-01

    FDA Recalls Methylcobalamin and Folic Acid Injectables Due to Sterility Concerns

    Axium Healthcare Pharmacy is recalling Methylcobalamin and Folic Acid Injectables because the products may lack sterility assurance.

    Product
    Methylcobalamin and Folic Acid Injectable Balanced Solutions, Compounding Pharmacy a division of Axium Healthcare Pharmacy, Inc., Lake Mary, FL 32746
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Devices)·Z-1131-2013·2013-04-24

    Heritage Labs Path Study Extra Supplies Kit Recalled for Contamination

    Heritage Labs is recalling 25 Path Study Extra Supplies Kits because they contain blood collection tubes with a Lithium Heparin contaminant that could cause erroneous lab results.

    Product
    Heritage Labs Path Study Extra Supplies Kit, Product # A 2376, kit contains 3 zippered plastic bags which hold support supplies for health care providers when treating patients. Bag #3 contains 5 different blood collection tubes (5 each) and 2 different gauge needles--all for dr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1045-2013·2013-04-10

    Zimmer NexPosure Retractor Portals Recalled for Sterility Risk

    Zimmer, Inc. is recalling 58 NexPosure retractor portals due to a potential breach in the sterile inner pouch, which could lead to product contamination and patient infection.

    Product
    Zimmer NexPosure, retractor portals of the NexPosure MIS Access System, Part Numbers or REF numbers: N1830R80-100, N1830R80-090¿, N1830R80-080¿, N1830R80-070¿, N1830R80-060, N1830R50-100, N1830R50-090, N1830R50-080, ¿ N1830R50-070, N1830R50-060, N1830L80-100, N1830L80-090, N1830L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2177-2013·2013-04-10

    Chu Minh Tofu Recalled Due to Lack of Hot Water in Facility

    Chu Minh Corp is recalling fresh and fried tofu products because they were produced in a facility without available hot water.

    Product
    CHU MINH TOFU Fresh Soybean Cake (Tofu), net weight 16 oz. The UPC is 8 18140 00002 2. The product is labeled in parts: "***CHUMINH TOFU***Fresh Soybean Cake (Tofu)***Ingredients: Soybean, Water, Calcium Sulfate***NET WT. 16 OZ***Perishable***Keep Refrigerated***CHUMINH TOFU
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·F-1284-2013·2013-04-10

    TJX Recalls Mrs. Bridges Scottish Raspberry Preserve Due to Contaminants

    The TJX Companies is recalling Mrs. Bridges Scottish Raspberry Preserve due to the discovery of contaminants. The product was distributed nationwide in 12 states and Puerto Rico.

    Product
    Mrs. Bridges Scottish Raspberry Preserve ("Jam"); Net Wt. 42g /1.5oz; service size 15g; servings per package: 2.8; ID 3779300377 Manufactured for: Kimm & Miller (UK) Ltd. mille Road, Bedford, MK429TW. United Kingdom; Manufacturer: Mackays Ltd., James Chalmers Road, Kirkton Ind E
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1021-2013·2013-04-03

    Microbiologics Recalls KWIK-QC Slides Due to Improper Fixation

    Microbiologics Inc is voluntarily recalling KWIK-QC Acid Fast and Mycobacterium slides because control organisms are not properly fixated, posing a contamination risk.

    Product
    Microbiologics KWIK-QC SLIDES ( KWIK-QC Acid Fast Stain Slides and KWIK-QC Mycobacterium Slides). Slide preparations serving as quality control challenges to demonstrate satisfactory performance of staining reagents.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Food)·F-1207-2013·2013-03-27

    Blue Planet 9 Grain Granola Recalled for Contaminated Ingredients

    Blue Planet Foods is recalling 9 Grain Granola because it contains two recalled Dakota Specialty Milling ingredients.

    Product
    Blue Planet, 10311 9 Grain Granola, NET WEIGHT 900 lbs (bulk product)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1203-2013·2013-03-27

    Blue Planet Foods Recalls Heartland Granola Cereals Due to Ingredient Issue

    Blue Planet Foods is recalling Heartland granola cereals because they contain two recalled Dakota Specialty Milling ingredients.

    Product
    Trio shipper which includes two of the recalled products: Heartland, AMERICA'S ORIGINAL, Harvest Spice Granola Cereal, NET WT 14 OZ. (397g), UPC 024300090394 and Heartland, AMERICA'S ORIGINAL, Fruit & Nut Harvest Granola Cereal, NET WT 14 OZ. (397g), UPC 024300090387
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1201-2013·2013-03-27

    Blue Planet Recalls Heartland Harvest Spice Granola Cereal Nationwide

    Blue Planet Foods is recalling Heartland Harvest Spice Granola Cereal because it contains two recalled Dakota Specialty Milling ingredients.

    Product
    Heartland, AMERICA'S ORIGINAL, Harvest Spice Granola Cereal, NET WT 14 OZ. (397g), UPC 024300090394
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1205-2013·2013-03-27

    Blue Planet Foods Recalls Pre-Baked Crisp Topping for Contaminated Ingredients

    Blue Planet Foods is recalling Orth Transmart Pre-Baked Crisp Topping because it contains two recalled Dakota Specialty Milling ingredients.

    Product
    #38605020 ORTH TRANSMART(TM) PRE-BAKED CRISP TOPPING, NET WEIGHT 30 LBS. (13.6 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1202-2013·2013-03-27

    Blue Planet Recalls Fruit and Nut Harvest Granola Cereal

    Blue Planet Foods is recalling Fruit & Nut Harvest Granola Cereal because it contains two recalled Dakota Specialty Milling ingredients.

    Product
    Heartland, AMERICA'S ORIGINAL, Fruit & Nut Harvest Granola Cereal, NET WT 14 OZ. (397g), UPC 024300090387
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1007-2013·2013-03-06

    Zip International Recalls Uneviscerated Dry Salted Fish

    Zip International Group is recalling dry salted fish found to be uneviscerated during NYSDAM sampling. The product was distributed in New York.

    Product
    Bream Dry Salted Fish Net Wt.: about 14.2 oz Imported by Zip International Group LLC Product of Russia
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-176-2013·2013-03-06

    Hospira Recalls 0.9% Sodium Chloride Irrigation Due to Sterility Concerns

    Hospira Inc. is recalling 56,854 units of 0.9% Sodium Chloride Irrigation, USP, 3000 mL, due to a potential leak from the administration port that compromises sterility.

    Product
    0.9% Sodium Chloride Irrigation, USP, 3000 mL, Sterile, Non pyrogenic, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7972-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0888-2013·2013-03-06

    Cellestis Recalls QuantiFERON TB Blood Collection Tubes Due to Contamination

    Cellestis is recalling QuantiFERON-TB Gold blood collection tubes due to potential contamination. The recall affects 309,400 units distributed worldwide.

    Product
    VACUETTE Cellestis 1 ml QuantiFERON¿ - TB ANTIGEN; Shake 10x; REF 454074; HE0105; 13X75 50 pcs.,1200 pcs. in total; Product Usage: QuantiFERON¿-TB Gold (QFT) is an in vitro diagnostic test using a peptide cocktail simulation ESAT-6, CFP-10 and TB7.7 (p4) proteins to stimulate
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0889-2013·2013-03-06

    Cellestis Recalls QuantiFERON TB Blood Collection Tubes Due to Contamination

    Cellestis is recalling QuantiFERON-TB Gold blood collection tubes due to potential contamination. The recall affects 29,690 units distributed worldwide.

    Product
    Vacuette Cellestis 1 ml QuantiFERON¿ TB ANTIGEN (HA) High Altitude: Shake 10x; REF 454413. HE0396. greiner bio-one; 13x75 50pcs.,1200 pcs in total. Product Usage: QuantiFERON¿-TB Gold (QFT) is an in vitro diagnostic test using a peptide cocktail simulation ESAT-6, CFP-10 and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0799-2013·2013-02-20

    Fresenius Liberty Cycler Set Recalled for Leak and Contamination Risk

    Fresenius Medical Care is recalling 5,590 Liberty Cycler Sets due to a small risk of leaks that could contaminate dialysate and cause peritonitis.

    Product
    Fresenius Liberty Cycler Set Single Conn. Ext. DL. Part Number: 050-87216. Acute and chronic peritoneal dialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-157-2013·2013-02-13

    Bracco Recalls Isovue-370 Injection Syringes Due to Particulate Matter

    Bracco Diagnostic Inc. is recalling specific lots of Isovue-370 injection syringes because they contain particulate matter, including cellulose and polyvinyl fibers.

    Product
    Isovue -370 (Iopamidol) Injection 76%, Prefilled 10 x 75 mL (NDC 0270-1316-66), 10 x 100 mL (NDC 0270-1316-67), 10 x 125 mL (NDC 0270-1316-68) Power Injector Syringe, Rx Only, Manufactured for Bracco Diagnostics Inc., Princeton, NJ 08543 by Nycomed GmbH 78224 Singen (Germany).
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-158-2013·2013-02-13

    Bracco Recalls Isovue-300 Injection Syringes Due to Particulate Matter

    Bracco Diagnostic Inc. is recalling specific lots of Isovue-300 Injection syringes because they contain particulate matter identified as cellulose and polyvinyl fibers.

    Product
    Isovue -300 (Iopamidol) Injection 61% Prefilled, 10 x 100 mL Power Injector Syringe, Rx Only, Manufactured for Bracco Diagnostics Inc., Princeton, NJ 08543 by Nycomed GmbH 78224 Singen (Germany); NDC 0270-1315-67.
    Category
    Drug
    Distribution
    Distributed nationwide