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FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

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Showing 13,061–13,080 of 17,974 drug recalls

Drug Recall Terminated Historical recordClass II

Testosterone Cypionate (Complete Formula) 100 mg/mL, Injection, Bedford Pharmacy, 209 Route 101, Bedford, NH 03110, (603) 472-3919

by Bedford Pharmacy

Reason
Lack of assurance of sterility
Recall initiated
September 22, 2015
Reported by FDA
October 21, 2015
Distribution
NH, MA

View recall →

Drug Recall Terminated Historical recordClass II

Acetylcysteine 10% Opthalmic Solution, Bedford Pharmacy, 209 Route 101, Bedford, NH 03110, (603) 472-3919

by Bedford Pharmacy

Reason
Lack of assurance of sterility
Recall initiated
September 22, 2015
Reported by FDA
October 21, 2015
Distribution
NH, MA

View recall →

Drug Recall Terminated Historical recordClass II

Hydroxocobalamin 20 mg/mL Injection, Bedford Pharmacy, 209 Route 101, Bedford, NH 03110, (603) 472-3919

by Bedford Pharmacy

Reason
Lack of assurance of sterility
Recall initiated
September 22, 2015
Reported by FDA
October 21, 2015
Distribution
NH, MA

View recall →

Drug Recall Terminated Historical recordClass II

Methylcobalamin (Bacteriostatic) 1 mg/mL Injection, Bedford Pharmacy, 209 Route 101, Bedford, NH 03110, (603) 472-3919

by Bedford Pharmacy

Reason
Lack of assurance of sterility
Recall initiated
September 22, 2015
Reported by FDA
October 21, 2015
Distribution
NH, MA

View recall →

Drug Recall Terminated Historical recordClass II

P-P (COBAL) 30-2 /mL, Injection, Bedford Pharmacy, 209 Route 101, Bedford, NH 03110, (603) 472-3919

by Bedford Pharmacy

Reason
Lack of assurance of sterility
Recall initiated
September 22, 2015
Reported by FDA
October 21, 2015
Distribution
NH, MA

View recall →

Drug Recall Terminated Historical recordClass II

P-P-P (COBAL) 30-1-20/mL, Injection, Bedford Pharmacy, 209 Route 101, Bedford, NH 03110, (603) 472-3919

by Bedford Pharmacy

Reason
Lack of assurance of sterility
Recall initiated
September 22, 2015
Reported by FDA
October 21, 2015
Distribution
NH, MA

View recall →

Drug Recall Terminated Historical recordClass II

Methylcobalamin (preservative Free) 1 mg/mL Injection, Bedford Pharmacy, 209 Route 101, Bedford, NH 03110, (603) 472-3919

by Bedford Pharmacy

Reason
Lack of assurance of sterility
Recall initiated
September 22, 2015
Reported by FDA
October 21, 2015
Distribution
NH, MA

View recall →

Drug Recall Terminated Historical recordClass III

Meijer Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets per box, Dist. By Meijer Distribution Inc. 2929 Walker Avenue NW, Grand Rapids, MI 49544. NDC 41250-527-31, UPC 7 6023662291 8

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Wal-itin Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-coiunt tablets per box, (NDC 0363-0527-69, ITEM 367492,UPC 3 1191717021 3); and b) 30-count tablets per box, (NDC 0363-0527-31, ITEM 254166, UPC 3 191715562 ) Distributed by Walgreen Co., 200 Wilmot Road, Deerfield, IL 60015

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Sunmark loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box (NDC 49348-930-01, UPC 0 1093936544 6); and b) 30-count tablets per box (NDC 49348-930-44, UPC 0 1093934944 6) Distributed by McKesson, One Post Street, San Francisco, CA 94104

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Up&Up loratadine orally disintegrating tablets, USP, 10 mg, 30-count tablets per box, Distributed by Target Corp, Minneapolis, MN 55403; NDC 11673-527-31, UPC 3 5166052731 5

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

TopCare LORATIDINE ORALLY DISINTEGRATING TABLETS, , USP, 10 mg, packaged in a) Children's 10-count tablets per box (NDC 36800-528-69, UPC 0 3680010261 3); and b) 10-count tablets per box, (NDC 36800-527-69, UPC 0 3680008395 0); Distributed by Topco Associates, LLC, Elk Grove Village, IL 60007.

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Safeway Care Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) 10-count tablets per box (NDC 21130-527-69, UPC 3 2113076240 9); b) 30-count tablets per box (NDC 21130-527-31, UPC 3 2113076252 2) Distributed by Safeway Inc. PO BOX 99, Pleasanton, CA 94566

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Premier Value Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets per box; Distributed by Chain Drug Consortium, 3301 NW Boca Raton Blvd. Suite 101, Boca Raton, FL 33431, NDC 68016-527-31, UPC 8 4098601899 2

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Ohm Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets, Distributed by Ohm Laboratories, Inc. 1385 Livingston Avenue, North Brunswick, NJ 08902, NDC 51660-527-31, UPC 3 5166052731 5

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Major loratadine orally disintegrating tablets, USP, 10 mg, 10-count tablets per box, Distributed by Major Pharmaceuticals 31778 Enterprise Drive, Livonia, MI 48150, USA, NDC 0904-5806-15, UPC 3 0904580615 9

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Leader Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets per box, Distributed by Cardinal Health, Dublin, OH 43017, NDC 37205-745-65, UPC 0 9629512322 7

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

HEB Loratadine Orally Disintegrating Tablets, USP, 10 mg, 10-count tablets per box, Made with pride & care for HEB, San Antonio, TX 78204, Item code: 188330, UPC 0 4122081968 3

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Health Mart Pharmacy loratadine orally disintegrating tablets, USP, 10 mg, 10-count tablets per box, Distributed by: McKesson, One Post Street, San Francisco, CA 94104, NDC 62011-0073-1, UPC 0 5256913369 9

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Drug Recall Terminated Historical recordClass III

Good Neighbor Pharmacy Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) For kids 10-count tablets per box, NDC 24385-0161-52, ABC # 042-226, UPC 0 8770140650 8; b) For adults 10-count tablets, NDC 46122-0140-52, ABC# 059-535, UPC 0877014065546, Distributed by: AmerisourceBergen, 1300 Morris Drive, Chesterbrook, PA 19087

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recall initiated
July 28, 2015
Reported by FDA
October 21, 2015
Distribution
Nationwide.

View recall →

Data last updated:

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.