FDA Recall
Ongoing
Historical recordClass II
Bupropion Hydrochloride Extended-Release Tablets USP (XL), 300 mg, 30-count bottles, Rx Only, Mfd. by: Graviti Pharmaceuticals Private Limited, Sangareddy, Telangana, India, Dist. by: Rising Phar, NDC 16571-863-03.
by Graviti Pharmaceuticals Private Limited
- Reason
- Failed Tablet/Capsule Specifications
- Published
- October 29, 2025
- Distribution
- Nationwide
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FDA Recall
Ongoing
Historical recordClass II
Ketorolac Tromethamine Injection, USP, 60 mg/2 mL (30 mg/mL), 2 mL Single-Dose Vial, For Intramuscular Use Only, Rx only, Mfd. for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Mfd. by: ASPIRO PHARMA LIMITED, Telangana - 502281, INDIA., U.S. Contact Number: 1-866-495-1995, NDC 31722-307-25 (Carton), 31722-307-02 (Vial label).
by Aspiro Pharma Limited
- Reason
- Presence of Particulate Matter: Particulate matter identified as glass
- Published
- October 29, 2025
- Distribution
- Nationwide
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FDA Recall
Ongoing
Historical recordClass II
Medline, Alcohol Prep Pads (2-Ply Pad, 70% Isopropyl Alcohol), 100 eaches per box, 10 boxes per case (1,000 eaches per case), Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL, 60093 USA, NDC 55329-811-30.
by Medline Industries, LP
- Reason
- Subpotent Drug
- Published
- October 29, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 %, 5 mL (0.17 FL OZ) bottles, Manufactured for: SOLA PHARMACEUTICALS LLC, Baton Rouge, LA 70810, NDC 70512-0520-05
by USV Private Limited
- Reason
- Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.
- Published
- October 29, 2025
- Distribution
- Nationwide
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FDA Recall
Ongoing
Historical recordClass III
Cetirizine Hydrochloride Tablets USP 10 mg, 500 Tablets bottles, Manufactured by: Unique Pharmaceuticals Labs, (A Div. of J.B. Chemicals & Pharmaceuticals, Ltd.), Mumbai 400 030, India. Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, NDC 16571-402-50
by JB Chemicals and Pharmaceuticals Ltd
- Reason
- Tablet/Capsules Imprinted with Wrong ID
- Published
- October 29, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass III
Cetirizine Hydrochloride Tablets USP 10 mg, 100 Tablets bottles, Manufactured by: Unique Pharmaceuticals Labs, (A Div. of J.B. Chemicals & Pharmaceuticals, Ltd.), Mumbai 400 030, India. Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, NDC 16571-402-10.
by JB Chemicals and Pharmaceuticals Ltd
- Reason
- Tablet/Capsules Imprinted with Wrong ID
- Published
- October 29, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Gabapentin Capsules, USP, 100 mg, 10 Capsules (10 x 1 blister pack), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-6665-61 (Blister pack), NDC 55154-3363-0 (Outer Bag).
by The Harvard Drug Group LLC
- Reason
- Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
- Published
- October 29, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Gabapentin Capsules, USP, 100 mg, 100 Capsules (10 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-6665-61
by The Harvard Drug Group LLC
- Reason
- Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
- Published
- October 29, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
M.C.I. Foods, Inc.
- Product
- Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; U…
- Reason
- Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
- Published
- October 29, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
M.C.I. Foods, Inc.
- Product
- Cheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz;…
- Reason
- Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
- Published
- October 29, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
DEMERS FOOD GROUP LLC
- Product
- Scott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
- Reason
- Contains Linguine manufactured by Nate's Fine Foods LLC recalled for Listeria monocytogenes and implicated in ongoing outbreak
- Published
- October 29, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
ROLLING PIN BAKING COMPANY LLC
- Product
- Rolling Pin brand Dubai Style Chocolate; 17.64 oz stand up p…
- Reason
- Product does not declare wheat in the allergen statement.
- Published
- October 29, 2025
- Distribution
- Multiple states
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Southwind Foods LLC dba Great American Seafood Imports Co.
- Product
- Great American branded Frozen raw shrimp skewer; 1lb bag U…
- Reason
- Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- Published
- October 29, 2025
- Distribution
- Distribution includes 26 domestic retail…
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FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Southwind Foods LLC dba Great American Seafood Imports Co.
- Product
- Tovala branded Frozen raw phosphate free shrimp; 5oz IQF bag…
- Reason
- Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- Published
- October 29, 2025
- Distribution
- Distribution includes 26 domestic retail…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Southwind Foods LLC dba Great American Seafood Imports Co.
- Product
- Arctic Shores branded Frozen cooked salad shrimp; 6 oz bag…
- Reason
- Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- Published
- October 29, 2025
- Distribution
- Distribution includes 26 domestic retail…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Southwind Foods LLC dba Great American Seafood Imports Co.
- Product
- Arctic Shores; Best Yet; Great American; Master Catch brande…
- Reason
- Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- Published
- October 29, 2025
- Distribution
- Distribution includes 26 domestic retail…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass II
Southwind Foods LLC dba Great American Seafood Imports Co.
- Product
- Arctic Shores; Best Yet; Great American; Master Catch brande…
- Reason
- Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- Published
- October 29, 2025
- Distribution
- Distribution includes 26 domestic retail…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
The Kroger Co
- Product
- Smoked Mozzarella Penne Salad, packaged in plastic container…
- Reason
- Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
- Published
- October 29, 2025
- Distribution
- AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN,…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
The Kroger Co
- Product
- Basil Pesto Bowtie Pasta Salad, packaged in plastic containe…
- Reason
- Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
- Published
- October 29, 2025
- Distribution
- AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN,…
View recall →
FDA Recall
Ongoing
Historical recordClass II
Carbidopa, Levodopa, Entacapone Tablets, 25 mg/100 mg/200 mg, 100-count bottle, Rx Only, Manufactured for: Rising Pharma Holdings, Inc. East Brunswick, NJ, 08816, Manufactured by Suven Pharmaceuticals Limited, Pashamylaram, Telangana, 205307, India. NDC# 16571-691-01
by Rising Pharma Holding, Inc.
- Reason
- Product mix up: complaint received that sealed medication bottle contained Carbidopa, Levodopa, and Entacapone film-coated tablets (37.5 mg/150 mg/200 mg) instead of labelled lower strength Carbidopa, Levodopa, and Entacapone film-coated tablets (25 mg/100 mg/200 mg).
- Published
- October 22, 2025
- Distribution
- Nationwide
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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