FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Meijer Inc./Traffic Dept.
- Product
- FRESH FROM MEIJER MIXED FRUIT CUP 6 OZ, 6oz Clear plastic co…
- Reason
- potential risk of Salmonella
- Published
- November 18, 2020
- Distribution
- Meijer stores in Michigan, Ohio, Indiana…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Meijer Inc./Traffic Dept.
- Product
- FRESH FROM MEIJER FRUIT FRENZY BOWL LARGE BOWL, 40oz Clear p…
- Reason
- potential risk of Salmonella
- Published
- November 18, 2020
- Distribution
- Meijer stores in Michigan, Ohio, Indiana…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Meijer Inc./Traffic Dept.
- Product
- FRESH FROM MEIJER FRUIT TRAY, 49oz Clear plastic container,…
- Reason
- potential risk of Salmonella
- Published
- November 18, 2020
- Distribution
- Meijer stores in Michigan, Ohio, Indiana…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Meijer Inc./Traffic Dept.
- Product
- FRESH FROM MEIJER FRUIT TRAY WITH DIP, 49oz Clear plastic co…
- Reason
- potential risk of Salmonella
- Published
- November 18, 2020
- Distribution
- Meijer stores in Michigan, Ohio, Indiana…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Meijer Inc./Traffic Dept.
- Product
- FRESH FROM MEIJER MIXED MELON SLICES, 24oz Clear plastic con…
- Reason
- potential risk of Salmonella
- Published
- November 18, 2020
- Distribution
- Meijer stores in Michigan, Ohio, Indiana…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Meijer Inc./Traffic Dept.
- Product
- FRESH FROM MEIJER MELONS & BERRIES WITH DIP, 22oz Clear plas…
- Reason
- potential risk of Salmonella
- Published
- November 18, 2020
- Distribution
- Meijer stores in Michigan, Ohio, Indiana…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Meijer Inc./Traffic Dept.
- Product
- FRESH FROM MEIJER TRIPLE TREAT & MELON, 22oz Clear plastic c…
- Reason
- potential risk of Salmonella
- Published
- November 18, 2020
- Distribution
- Meijer stores in Michigan, Ohio, Indiana…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Meijer Inc./Traffic Dept.
- Product
- FRESH FROM MEIJER CANTALOUPE AND HONEYDEW SLICES, 24oz Clear…
- Reason
- potential risk of Salmonella
- Published
- November 18, 2020
- Distribution
- Meijer stores in Michigan, Ohio, Indiana…
View recall →
FDA Recall
🇺🇸 United States
Terminated
Historical recordClass I
Meijer Inc./Traffic Dept.
- Product
- FRESH FROM MEIJER CANTALOUPE CHUNKS LARGE BOWL, 32oz Clear p…
- Reason
- potential risk of Salmonella
- Published
- November 18, 2020
- Distribution
- Meijer stores in Michigan, Ohio, Indiana…
View recall →
FDA Recall
Terminated
Historical recordClass II
Lansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg, 100-count carton (10 x10 unit-dose), Rx only, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534, NDC 68382-772-77
by Zydus Pharmaceuticals (USA) Inc
- Reason
- Failed Dissolution Specification
- Published
- November 11, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg, 100-count carton (10 x10 unit-dose), Rx only, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534, NDC 68382-771-77
by Zydus Pharmaceuticals (USA) Inc
- Reason
- Failed Dissolution Specification
- Published
- November 11, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, 100 count bottles, Rx Only. Manufactured by: Nostrum Laboratories, Inc. Kansas City, MO 64120. NDC 29033-055-01
by Nostrum Laboratories Inc
- Reason
- CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
- Published
- November 11, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count bottles, Rx Only. Manufactured by: Nostrum Laboratories, Inc. Kansas City, MO 64120. NDC 29033-056-01
by Nostrum Laboratories Inc
- Reason
- CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
- Published
- November 11, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Olanzapine Orally Disintegrating Tablets, 5 mg, 30 count (3x10 unit dose) blister pack, Rx only, Manufactured by: Jubilant Generics, Ltd., Roorkee, India, Marketed by: Jubilant Cardista Pharmaceuticals, Inc., Salisbury, MD NDC 59746-0306-32
by Jubilant Cadista Pharmaceuticals, Inc.
- Reason
- Subpotent
- Published
- November 11, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass III
Fluocinonide Ointment USP 0.05%, packaged in: a) 15 gm tube, NDC 52565-0040-15, b) 30 gm tube, NDC 52565-0040-30 c) 60 gram tube, NDC 52565-0040-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310
by Teligent Pharma, Inc.
- Reason
- Failed Impurities/Degradation - Out-of-specification results for Fluocinolone Acetonide impurity.
- Published
- November 11, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Time-Cap Labs, Inc. Metformin Hydrochloride Extended Release Tablets USP 750 mg, 100 count bottles, Rx Only Manufactured for: Time-Cap Labs, Inc. 7 Michael Avenue Farmingdale, NY 11735, USA Manufactured by: Marksans Pharma Ltd. Plot No. L-82, L-83, Verna Indl. Estate. Verna Goa-403 722 India NDC 49483-624-01
by Marksans Pharma Limited
- Reason
- CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
- Published
- November 11, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
Time-Cap Labs, Inc. Metformin Hydrochloride Extended-Release Tablets USP 500 mg, a) 90 count (NDC 49483-623-09) b) 100 count (49483-623-01) c) 500 count (NDC 49483-623-50) and d) 1000 count (NDC 49483-623-10) bottles, Rx Only Manufactured for: Time-Cap Labs, Inc. 7 Michael Avenue Farmingdale, NY 11735, USA, Manufactured by: Marksans Pharma Ltd. Plot No. L-82, L-83, Verna Indl. Estate. Verna Goa-403 722 India NDC 49483-623-50
by Marksans Pharma Limited
- Reason
- CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
- Published
- November 11, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, a) 30 count (NDC 70934-309-30); b) 60 count (NDC 70934-309-60); c) 90 count (70934-309-90); d) 120 count (NDC 70934-309-98) bottles, Rx Only, Time-Cap Labs Inc. Repackaged by Northwind Pharmaceuticals North Blenheim, NY 12131
by Denton Pharma, Inc.
- Reason
- CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)
- Published
- November 11, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Ongoing
Historical recordClass II
Metformin Hydrochloride Extended-Release Tablets USP 750 mg, 30 Tablets bottle, Rx Only, Time-Cap Labs, Inc., Repackaged By: Northwind Pharmaceuticals North Blenheim NY 12131 NDC 70934-334-30
by Denton Pharma, Inc.
- Reason
- CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)
- Published
- November 11, 2020
- Distribution
- Nationwide
View recall →
FDA Recall
Terminated
Historical recordClass II
N-A-C (N-Acetyl-L-Cysteine, 500 mg, 100 capsules; Veggie Caps, white HDPE bottle with RED label Product # 107002 UPC: 790011070023
by Jarrow Formulas Inc
- Reason
- Mislabeling of SUS (N-A-C Sustain 600 mg 100 tab) with N-A-C N-Acetyl-L-Cysteine 500 mg, 100 cap.
- Published
- November 4, 2020
- 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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