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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to October 2026.

37,205
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,841
Class I recallsReasonable probability of serious health consequences
24,366
Class II recallsTemporary or medically reversible health consequences
2,892
Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls
Most common hazardLack of Assurance of Sterility 2,073 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible-0Published October 1, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,714 recalls have been announced year to date.
  • Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
  • Oct 2026 is incomplete and not included in the figures above.
  • Complete data
  • Incomplete
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 15,261–15,280 of 18,765 recalls

FDA 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
Published
October 21, 2015
Distribution
NH and MA

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FDA 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
Published
October 21, 2015
Distribution
NH and MA

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FDA 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
Published
October 21, 2015
Distribution
NH and MA

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FDA 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
Published
October 21, 2015
Distribution
NH and MA

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FDA 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
Published
October 21, 2015
Distribution
NH and MA

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FDA 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
Published
October 21, 2015
Distribution
NH and MA

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FDA 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.
Published
October 21, 2015
Distribution
Nationwide

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FDA 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.
Published
October 21, 2015
Distribution
Nationwide

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FDA 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.
Published
October 21, 2015
Distribution
Nationwide

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FDA 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.
Published
October 21, 2015
Distribution
Nationwide

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FDA 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.
Published
October 21, 2015
Distribution
Nationwide

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FDA 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.
Published
October 21, 2015
Distribution
Nationwide

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FDA 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.
Published
October 21, 2015
Distribution
Nationwide

View recall →

FDA 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.
Published
October 21, 2015
Distribution
Nationwide

View recall →

FDA 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.
Published
October 21, 2015
Distribution
Nationwide

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FDA 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.
Published
October 21, 2015
Distribution
Nationwide

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FDA 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.
Published
October 21, 2015
Distribution
Nationwide

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FDA 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.
Published
October 21, 2015
Distribution
Nationwide

View recall →

FDA 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.
Published
October 21, 2015
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Fred's Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-counts tablets per box, Distributed by: fred's, Inc., 4300 New Getwell Road, Memphis, TN 38118, UPC 0 8457912198 4.

by Ohm Laboratories, Inc.

Reason
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Published
October 21, 2015
Distribution
Nationwide

View recall →

Data last updated:

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. Read the full medical disclaimer.