Hazard

Contamination recalls

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

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.

76–100 of 684

HighFDA (Drugs)·D-0170-2026·2025-11-26
Lantiseptic Skin Protectant Recalled Due to Facility Manufacturing Deviation
DermaRite Industries is recalling Lantiseptic Skin Protectant nationwide due to manufacturing practice deviations at a facility where contamination was found in other product lots.
Product
Lantiseptic, Skin Protectant, Lanolin USP 30%, packaged in a) 5g (0.17 oz) (NDC 61924-304-05), b)14.2g (0.5 oz)( NDC 61924-304-14), c) 4oz (NDC 61924-304-04), d) 4.5oz (NDC 61924-304-45), and e) 12oz (NDC 61924-304-12) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0177-2026·2025-11-26
UltraSure Anti-Perspirant and Deodorant Recalled for Manufacturing Facility Contamination
DermaRite Industries is recalling UltraSure Anti-Perspirant & Deodorant (118 mL spray) due to manufacturing facility contamination affecting all lots nationwide with expiration dates through August 2027.
Product
UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl. oz.), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-266-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0162-2026·2025-11-26
Antifungal Cream Recall Due to Manufacturing Facility Contamination
DermaFungal Antifungal Cream is being recalled because it was manufactured at a facility with CGMP violations and confirmed contamination of other products. The recall affects all lots distributed nationwide.
Product
DermaFungal, Antifungal Cream with 2% Miconazole Nitrate, packaged in a) 5 g (0.18 oz) per packet (NDC 61924-234-05), and b)106 g (3.75 oz.) per tube (NDC 61924-234-04) DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0160-2026·2025-11-26
DermaRite 4-N-1 Skin Protectant Recalled for Manufacturing Facility Deviation
DermaRite Industries recalls 4-N-1 Skin Protectant nationwide due to manufacturing facility contamination. Consumers should stop using the product.
Product
4-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone 1%, 113g, (4 oz) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-208-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0176-2026·2025-11-26
San-E-Foam Antiseptic Foam Recalled Due to Facility Contamination
San-E-Foam antiseptic foam is recalled due to manufacturing facility contamination. All lots through August 2027 distributed nationwide are affected.
Product
San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-107-34
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0308-2026·2025-11-05
Alcon Surgical Accessory Devices Recalled for Incomplete Pouch Seals
Alcon is recalling approximately 1632 surgical accessory devices used in eye surgery due to incomplete seals in sterile packaging pouches. The affected devices are distributed worldwide.
Product
Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065000356 27GA HP ENTRY SYSTEM, 4 MM 1 COUNT 8065000358 25GA HP ENTRY SYSTEM, 6 MM 1 COU
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0317-2026·2025-11-05
Magnetic surgical marker recalled due to potential cotton fiber contamination
Endomagnetics Ltd is recalling 540 units of Magseed Pro magnetic surgical markers due to potential cotton fiber contamination. The devices are used to mark soft tissue during surgical procedures.
Product
Magseed Pro 12 cm soft tissue marker. Model Number: MS2-17-1-12. Product Description: The Endomag Magseed Pro Magnetic Marker System is a sterile, single use device composed of a marker preloaded in a 17ga Needle Delivery System. The Endomag Magseed Pro Marker is indicated for
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0104-2026·2025-11-05
Teva Recalls Prazosin Hydrochloride Capsules for Carcinogenic Impurity
Teva Pharmaceuticals recalls Prazosin Hydrochloride 1 mg capsules nationwide due to N-nitroso impurity levels exceeding FDA acceptable limits. Patients should consult their healthcare provider.
Product
PRAZOSIN HYDROCHLORIDE — PRAZOSIN HYDROCHLORIDE (PRAZOSIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0304-2026·2025-11-05
Alcon Surgical Console Probes Recalled for Incomplete Sterile Packaging Seals
Alcon is recalling 577 accessory devices used with its surgical consoles due to incomplete seals in sterile packaging pouches. The incomplete seals may compromise the sterile barrier required for safe vitrectomy surgical procedures.
Product
Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065000250 UNITY 27+DS HYPERVIT 30K VIT PROBE 8065753168 UNITY 25+ 7.5K ANTERIOR VIT PROB
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0411-2026·2025-11-05
Ophthalmic knife with contaminated suction set springs recalled for potential eye irritation
MicroSurgical Technology Inc is recalling the MST ArcDUO 9mm ophthalmic knife after contamination was found in the suction set springs. The unidentified residue may potentially cause eye irritation.
Product
MST ArcDUO 9mm, REF: ARC-0002, single-use, sterile ophthalmic knife, used with Suction Set, Part: 48-1000-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0112-2026·2025-11-05
Desipramine Hydrochloride Tablets Recalled for N-Nitroso Impurity
Heritage Pharmaceuticals is recalling Desipramine Hydrochloride 150 mg tablets nationwide due to N-Nitroso impurity contamination exceeding acceptable safety levels. Affected patients should consult their healthcare provider.
Product
DESIPRAMINE HYDROCHLORIDE — DESIPRAMINE HYDROCHLORIDE (DESIPRAMINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0309-2026·2025-11-05
Aesculap Surgical Trocar Sealing Unit Recalled for Potential Silicone Fragmentation
Aesculap is recalling a trocar sealing unit (Model EK083P) because silicone fragments may detach from the yellow sealing component. Affected units were distributed in the US and Canada.
Product
Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software Version: N/A Product Description: SEALING UNIT F/10/12MM TROCARS W.REDUCER Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0117-2026·2025-10-29
Albertsons Ready Meals Pesto Bowtie Pasta Salad recalled for Listeria
Albertsons is recalling Ready Meals Pesto Bowtie Pasta Salad due to Listeria monocytogenes contamination in the pasta ingredient. Affected products were sold at multiple store banners from September 8 to October 4, 2025.
Product
READY MEALS Pesto Bowtie Pasta Salad, UPC 27133 #####. Product was made in-store with store generated scale label applied to the container. Sold under store banners Albertsons, Pavilions, Randalls, Safeway, Tom Thumb, and Vons in AR, AZ, CA, CO, LA, NE, NM, NV, OK, SD, TX, UT
Category
Food
Distribution
15 states
SevereFDA (Food)·H-0150-2026·2025-10-29
Ready-to-Eat Egg Breakfast Products Recalled for Listeria Monocytogenes
M.C.I. Foods is recalling ready-to-eat egg breakfast products because the cooked egg ingredient tested positive for Listeria monocytogenes. The recall covers 1,040 cases distributed to institutional food buyers.
Product
Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.50 oz; 72 count/case; UPC# 1 070657 497861 1
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0097-2026·2025-10-29
Drug vials recalled due to lack of sterility assurance
Bristol-Myers Squibb is recalling 12,778 vials of Opdualag (an immunotherapy drug) nationwide due to lack of assured sterility.
Product
OPDUALAG — OPDUALAG (NIVOLUMAB AND RELATLIMAB-RMBW)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0028-2026·2025-10-22
FASENRA (Benralizumab) Injectable Drug Recall Due to Sterility
AstraZeneca is recalling FASENRA (benralizumab) pre-filled syringes due to lack of assurance of sterility. Patients who received injections from the recalled lot should contact their healthcare provider.
Product
FASENRA — FASENRA (BENRALIZUMAB)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0057-2026·2025-10-15
L-Carnitine for Injection Recall Due to Lack of Sterility Assurance
GenoGenix LLC is recalling all lots of L-Carnitine for Injection due to lack of assurance of sterility. The affected product was distributed nationwide in the United States.
Product
L-Carnitine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0045-2026·2025-10-15
B6 Injection Recall: FDA Class II Alert for Sterility Concerns
FDA recalls all lots of B6 (Pyridoxine HCl) for Injections manufactured by GenoGenix LLC due to lack of sterility assurance. The injectable product is distributed nationwide.
Product
B6 (Pyridoxine HCl) for Injections, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Synergy Wellness
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0093-2026·2025-10-15
Retatrutide for Injection recalled for sterility assurance failure
GenoGenix LLC is recalling Retatrutide for Injection 60mg vials due to lack of assurance of sterility. The affected lot was distributed nationwide.
Product
Retatrutide for Injection, 60mg / 10mL vial, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0040-2026·2025-10-15
Ascorbic Acid for Injection Recalled for Lack of Sterility Assurance
GenoGenix is recalling all lots of Ascorbic Acid (Vitamin C) for Injection due to lack of assurance of sterility. The product was distributed nationwide.
Product
Ascorbic Acid (Vitamin C) for Injection, Preservative Free, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0042-2026·2025-10-15
B12 Hydroxocobalamin Injectable Drug Recalled Nationwide for Sterility Assurance
GenoGenix LLC recalls B12 Hydroxocobalamin for Injection nationwide due to lack of assurance of sterility. The injectable pharmaceutical is affected in all lots currently within expiration.
Product
B12 Hydroxocobalamin for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0078-2026·2025-10-15
Pentosan for Injection recalled due to sterility assurance failure
GenoGenix is recalling all unexpired lots of Pentosan for Injection due to lack of assurance of sterility. The affected product has been distributed nationwide throughout the United States.
Product
Pentosan for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0020-2026·2025-10-08
NES Laser Atherectomy Catheter Recalled for Sterile Packaging Breach Risk
Northeast Scientific is recalling 165 units of the NES Reprocessed Laser Atherectomy Catheter due to potential breaches in sterile barrier packaging that could compromise sterility assurance.
Product
NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-152. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cl
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0629-2025·2025-10-01
Middlefield Smoked Cheddar Cheese Recalled for Potential Listeria Contamination
Middlefield Original Cheese Cooperative is recalling Smoked Cheddar cheese due to potential Listeria monocytogenes contamination. The recall affects 364.125 cases distributed to OH, PA, WI, and TX.
Product
Middlefield Original Cheese Co-op Smoked Cheddar, 5 lb. loaves, packaged 8 loaves per case
Category
Food
Distribution
4 states
ModerateFDA (Drugs)·D-0673-2025·2025-10-01
Amphetamine capsules recalled for failed impurity and degradation specifications
Granules Pharmaceuticals Inc. is recalling dextroamphetamine mixed salts extended-release 30 mg capsules nationwide due to failed impurity and degradation specifications. Consumers should contact their pharmacist or doctor for guidance.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide