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.

301–325 of 2096

  • HighFDA (Devices)·Z-0343-2024·2023-11-29

    Small intestinal videoscope recalled due to inadequate channel drying process

    Aizu Olympus is recalling small intestinal videoscopes (Model SIF-Q180) because the channel air drying process was not properly validated. Water remaining in the channels could cause contamination and infection risk.

    Product
    Small intestinal videoscope-For endoscopy and endoscopic surgery within the upper digestive tract (including the esophagus, stomach, duodenum, and small intestine) by oral insertion or the lower digestive tract (including the anus, rectum, sigmoid colon, colon, ileocecal valve…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0340-2024·2023-11-29

    Mobile Airway Scope Recalled Due to Unvalidated Drying Process

    Aizu Olympus has recalled 33 Mobile Airway Scope units due to an unvalidated air drying process. Some repaired units had wet channels, creating a potential risk of contamination and infection.

    Product
    Mobile airway scope-diagnosis and observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: MAF-DM2, MAF-GM, MAF-GM2, MAF-TM, MAF-TM2.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0346-2024·2023-11-29

    Olympus endoscopes recalled for potential water contamination in channels

    Aizu Olympus Co., Ltd. is recalling duodenovideoscope models due to an unvalidated channel air drying process. Water remaining in the channels after repair poses a potential contamination risk that could lead to infection.

    Product
    Duodenovideoscope-EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery Model Numbers: TJF-145, TJF-150, TJF-Q180V, TJF-Q190V.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0332-2024·2023-11-29

    Rhinolaryngoscope Models Recalled for Unvalidated Air Drying Process

    Aizu Olympus rhinolaryngoscopes (models ENF-T3, ENF-VT2, ENF-VT3) are recalled. The air-drying process for the instrument channel was not validated, and water remaining in some devices after repair poses contamination and infection risk.

    Product
    Rhinolaryngoscope-for endoscopic diagnosis and treatment within the nasal lumens and airway anatomy (including nasopharyngeal and trachea). Model Numbers: ENF-T3, ENF-VT2, ENF-VT3.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0328-2024·2023-11-29

    Ultrasonic Bronchoscopes Recalled Due to Inadequate Drying Validation

    Aizu Olympus is recalling 823 ultrasonic bronchoscopes (models BF-UC180F, BF-UC190F) because the channel air drying process was not validated, and some repaired units retained water that could cause contamination and infection.

    Product
    Bronchoscope - Ultrasonic: endoscopic real-time ultrasonic imaging, ultrasound guided needle aspiration and other endoscopic procedures within the airways, trancheobronchial tree, esophagus and surrounding organs Model Numbers: BF-UC180F, BF-UC190F.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0337-2024·2023-11-29

    Hysterofiberscope Model HYF-XP Channel Drying Process Flaw Poses Infection Risk

    Aizu Olympus is recalling HYF-XP hysterofiberscopes because the channel air drying process was not validated. Some repaired units have wet channels that could harbor contamination and pose infection risk.

    Product
    Hysterofiberscope-For endoscopic diagnosis within the uterus. Model Number: HYF-XP.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0307-2024·2023-11-22

    Medical Device Recall: KWIKSTIK Microbiological Reagent Contaminated with Aspergillus

    Microbiologics Inc recalls KWIKSTIK microbiological reagent kits due to Aspergillus flavus contamination in bulk pellets. Affected products were distributed worldwide, including the US, Italy, France, Turkey, Peru, and Mexico.

    Product
    KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0057-2024·2023-10-25

    Cefuroxime Injectable Syringes Recalled for Lack of Sterility Assurance

    Pine Pharmaceuticals is recalling 4,972 syringes of Cefuroxime injectable medication due to lack of assurance of sterility. The compounded antibiotic was distributed nationwide.

    Product
    Cefuroxime 4mg /0.4 mL (10 mg/mL), 1mL syringe, Rx only, Compounded by: Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0035-2024·2023-10-18

    Hemodialysis Systems Recalled for Potential PCBA Tubing Leaching

    Fresenius Medical Care is recalling 733 hemodialysis machines nationwide due to potential leaching of circuit board material from tubing. Affected equipment may contaminate blood or dialysate during treatment.

    Product
    2008T HD SYS. W/O CDX W/BIBAG BLUESTAR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0009-2024·2023-10-11

    Fentanyl Injectable Solution Recalled for Sterility Assurance Defect

    Central Admixture Pharmacy Services is recalling fentanyl 10 mcg/mL injectable solution due to lack of assurance of sterility. The recall affects 1,767 three-milliliter syringes distributed nationwide.

    Product
    fentaNYL in 0.9% sodium chloride, 10 mcg/1 mL, (10 mcg/mL), 3 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C San Diego, CA 92126, NDC: 71286-2071-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0025-2024·2023-10-11

    BD Cathena IV Catheter Safety Shield May Fail to Properly Engage

    Becton Dickinson is recalling BD Cathena IV catheters because the safety shield may fail to properly engage, potentially exposing the contaminated needle.

    Product
    REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min , Rx Only, Sterile EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0024-2024·2023-10-11

    Fentanyl in Dextrose Syringes Recalled for Sterility Assurance Issues

    Central Admixture Pharmacy Services is recalling 962 fentanyl in dextrose syringes distributed nationwide due to lack of assured sterility in the injectable pharmaceutical products.

    Product
    fentaNYL in dextrose 5%, 300 mcg/30 mL, (10 mcg/mL), 30 mL syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2001-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0001-2024·2023-10-11

    Fentanyl Injectable Syringes Recalled for Lack of Sterility Assurance

    Central Admixture Pharmacy Services Inc. is recalling 1,762 fentanyl syringes nationwide due to lack of assurance of sterility. No illnesses or injuries have been reported.

    Product
    fentaNYL in 0.9% sodium chloride, 10 mcg/1 mL, (10 mcg/mL), 3 mL syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2071-7
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0019-2024·2023-10-11

    Fentanyl Injectable Syringes Recalled Due to Sterility Assurance Issue

    Central Admixture Pharmacy Services is recalling fentanyl 100 mcg/2 mL syringes due to a lack of assurance of sterility. The affected lot was distributed nationwide.

    Product
    fentaNYL, 100 mcg/2 mL, (50 mcg/mL), 3 mL Syringe, Rx only, Repackaged by CAPS Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2003-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1630-2023·2023-10-04

    Sorbet Layer Cake Recalled for Potential Listeria Contamination

    ICE CREAM HOUSE recalled a 10'' Sorbet 4 Layer Cake for potential Listeria monocytogenes contamination. Distribution was in Ohio, New Jersey, and New York.

    Product
    10'' Sorbet 4 Layer Cake; parve; 1 PACK; UPC: 0-91404-15111-5
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1612-2023·2023-10-04

    Regal Foods recalls Herbs De Provence seasoning for rodent feces contamination

    Regal Foods is recalling Regal Herbs De Provence seasoning after rodent feces were found in oregano samples. The product was distributed in Georgia, Maryland, Pennsylvania, and Kentucky.

    Product
    REGAL HERBS DE PROVENCE 2# various containers.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1552-2023·2023-10-04

    Fenugreek Capsule Recall Due to Pen Pieces Contamination

    Vitality Works is recalling 1,025 bottles of 100 vegetarian Fenugreek Capsules due to contamination with pieces of a writing pen. The product was distributed to 55 retail customers across 284 stores in the United States.

    Product
    100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1610-2023·2023-10-04

    Regal Foods Recalls Herbs and Garlic Due to Rodent Contamination

    Regal Foods is recalling 660 pounds of herbs and garlic products distributed to GA, MD, PA, and KY after rodent feces were found in oregano samples. Consumers should dispose of affected products marked with code 8400.

    Product
    REGAL HERBS & GARLIC 25# 5# 2# various containers.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1613-2023·2023-10-04

    Regal Foods Recalls Oregano Seasoning Due to Rodent Contamination

    Regal Foods, Inc is recalling REGAL PASTA HERB 4oz packages due to rodent feces found in oregano samples. The product was distributed to GA, MD, PA, and KY.

    Product
    REGAL PASTA HERB 4oz, various containers.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0005-2024·2023-10-04

    Cerebelly Smart Bars recalled for visible surface mold

    Cerebelly Inc is recalling Cerebelly Smart Bars (Carrot Date flavor, 5-pack) due to visible mold on the product surface. The recall affects products distributed across all 50 U.S. states and territories.

    Product
    Cerebelly Smart Bar; Carrot Date flavor; 5 pk; ambient storage
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1548-2023·2023-10-04

    Fenugreek Capsules Recalled for Foreign Material Contamination

    Vitality Works Inc is recalling 100 Vegetarian Fenugreek Capsules due to pen fragments found in the product. The recall affects approximately 1,025 bottles distributed across 284 retail stores in the United States.

    Product
    100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1579-2023·2023-10-04

    Vitality Works Fenugreek Capsules Recalled for Foreign Material

    Vitality Works is recalling 1,025 bottles of 100-count Fenugreek Capsules (600mg) due to contamination with pieces of a pen. The recall affects 284 retail locations across the United States.

    Product
    100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1594-2023·2023-10-04

    Fenugreek Capsule Supplement Recalled for Pen Piece Contamination

    Vitality Works is recalling 1,025 bottles of 100-count Fenugreek Capsules (600mg) due to contamination with pen pieces. The affected lot is 2023-06871, distributed to stores across the United States.

    Product
    100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1614-2023·2023-10-04

    Regal Blackening Season recalled for rodent feces contamination

    Regal Foods, Inc. is recalling Regal Blackening Season seasoning due to rodent feces found in oregano samples. The product was distributed to Georgia, Maryland, Pennsylvania, and Kentucky.

    Product
    REGAL BLACKENING SEASON 5#, various containers.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0004-2024·2023-10-04

    Cerebelly Smart Bars recalled due to visible surface mold

    Cerebelly Inc is recalling Cerebelly Smart Bar in Blueberry Banana flavor due to visible surface mold. The recall affects 154,554 cases distributed to all 50 U.S. states and territories.

    Product
    Cerebelly Smart Bar; Blueberry Banana flavor; 5 pk; ambient storage
    Category
    Food
    Distribution
    0 states