FDA Recall
🇺🇸 United States
Completed
2026 recordClass I
Ambriola Co., Inc., The
- Product
- Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup…
- Reason
- Product tested positive for Listeria Monocytogenes.
- Published
- January 14, 2026
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
Completed
2026 recordClass I
Ambriola Co., Inc., The
- Product
- Ambriola Piccante grated Pecorino Romano, 5 and 10-pound pla…
- Reason
- Product tested positive for Listeria Monocytogenes.
- Published
- January 14, 2026
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
Completed
2026 recordClass I
Ambriola Co., Inc., The
- Product
- Boar's Head Pecorino Romano Grated, 5-pound plastic bag (uni…
- Reason
- Product tested positive for Listeria Monocytogenes.
- Published
- January 14, 2026
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
Completed
2026 recordClass I
Ambriola Co., Inc., The
- Product
- Sam's Pecorino Romano grated, 1.5 lb Plastic Bags, 12 units…
- Reason
- Product tested positive for Listeria Monocytogenes.
- Published
- January 14, 2026
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
Completed
2026 recordClass I
Ambriola Co., Inc., The
- Product
- Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid,…
- Reason
- Product tested positive for Listeria Monocytogenes.
- Published
- January 14, 2026
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
Completed
2026 recordClass I
Ambriola Co., Inc., The
- Product
- Pinna Grated Pecorino Romano 2/10, 10-pound plastic bags (un…
- Reason
- Product tested positive for Listeria Monocytogenes.
- Published
- January 14, 2026
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
Completed
2026 recordClass I
Ambriola Co., Inc., The
- Product
- Locatelli Grated Pecorino Romano, 5 and 10-pound plastic bag…
- Reason
- Product tested positive for Listeria Monocytogenes.
- Published
- January 14, 2026
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
Completed
2026 recordClass I
Ambriola Co., Inc., The
- Product
- Locatelli Grated Pecorino Romano 4 oz and 8 oz plastic cup &…
- Reason
- Product tested positive for Listeria Monocytogenes.
- Published
- January 14, 2026
- Distribution
- The recalled product was distributed to…
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FDA Recall
🇺🇸 United States
Terminated
2026 recordClass II
D. Coluccio & Sons Inc.
- Product
- Sapori Amaretti Almonds 175 g Cookies
- Reason
- Contains elevated levels of hydrocyanic acid
- Published
- January 14, 2026
- Distribution
- Multiple states
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FDA Recall
🇺🇸 United States
Ongoing
2026 recordClass II
Town Food Service Equip Co Inc
- Product
- Town Food Service EQ CO Inc. brand Aluminum Sauce Pans in 1Q…
- Reason
- Product found to contain leachable lead levels.
- Published
- January 14, 2026
- Distribution
- AL, AR, AZ, CA, CO, FL, GA, IL, KY, LA,…
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FDA Recall
Ongoing
2026 recordClass III
traZODONE Hydrochloride Tablets, USP, 100mg, 1,000 Tablets, Rx only, Manufactured by: Zydus Lifesciences Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-806-10
by Zydus Pharmaceuticals (USA) Inc
- Reason
- Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface.
- Published
- January 7, 2026
- Distribution
- Nationwide
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FDA Recall
Ongoing
2026 recordClass II
Ondansetron Orally Disintegrating Tablets, USP, 4mg, 30 Tablets (3 blistercards each containing 10 tablets), Rx only, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430, Product of India, NDC 68462-157-13
by Glenmark Pharmaceuticals Inc., USA
- Reason
- Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale.
- Published
- January 7, 2026
- Distribution
- Nationwide
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FDA Recall
Ongoing
2026 recordClass II
Wegovy (semaglutide) Injection, 1 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880 Bagsvaerd, Denmark, Product of Denmark, Novo Nordisk A/S, Novo Nordisk Inc., Plainsboro, NJ 08536, NDC 0169-4501-14
by Novo Nordisk Inc.
- Reason
- Presence of Particulate Matter: Hair was found in a prefilled syringe
- Published
- January 7, 2026
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
2026 recordClass II
Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880 Bagsvaerd, Denmark, Product of Denmark, Novo Nordisk A/S, Novo Nordisk Inc., Plainsboro, NJ 08536, NDC 0169-4505-14
by Novo Nordisk Inc.
- Reason
- Presence of Particulate Matter: Hair was found in a prefilled syringe
- Published
- January 7, 2026
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
2026 recordClass II
BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), 2% w/v and Isopropyl alcohol (IPA), 70% v/v), 5.25 mL Applicator, CareFusion 213, LLC, El Paso, TX 79912, NDC 54365-401-29
by CareFusion 213, LLC
- Reason
- Lack of Assurance of Sterlity
- Published
- January 7, 2026
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
Ongoing
2026 recordClass II
Tom Bumble LLC
- Product
- Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Cho…
- Reason
- Foreign material.
- Published
- January 7, 2026
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Ongoing
2026 recordClass II
INDIAN COOKWARE AND APPLIANCE LLC
- Product
- ALUMINIUM HAMMERED KADAI SIZE 7 8 901000 000057 MADE IN INDI…
- Reason
- Potential contamination due to leachable lead.
- Published
- January 7, 2026
- Distribution
- U.S. Distribution: CA
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FDA Recall
Ongoing
Historical recordClass II
Noxafil Powdermix (posaconazole) for Delayed-Release Oral Suspension, 300 mg, 8 packets per carton, Rx Only, Manufactured for: Merck Sharp & Doohme LLC, Rahway, NJ 07056 USA, Manufactured by: N.V. Organon, 5349 AB Oss, The Netherlands, a subsidiary of Organon & Co., Jersey City, NJ 07302, USA NDC 0085-2224-02.
by Merck Sharp & Dohme LLC
- Reason
- Presence of particulate matter: potential presence of metal particulates in the product.
- Published
- December 31, 2025
- Distribution
- Nationwide
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FDA Recall
Ongoing
Historical recordClass II
Merck Emend (aprepitant) for oral suspension, 125 mg, Single-Dose Kit, Rx Only, Manufactured for: Merck Sharpe & Dohme LLC, Rahway, NJ 07065, USA, Manufactured by: Novo Nordisk Production Ireland Limited Athlone, Ireland, NDC 0006-3066-03
by Merck Sharp & Dohme LLC
- Reason
- Presence of particulate matter: potential presence of metal particulates in the product.
- Published
- December 31, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Ongoing
Historical recordClass II
A New Life Herbs, LLC
- Product
- Sinus Cap Herbal Supplement, Herbs containing antibiotic, dr…
- Reason
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Published
- December 31, 2025
- Distribution
- Multiple states
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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