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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 September 2026.

37,115
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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 2,072 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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)

  • 1,527 recalls have been announced year to date.
  • Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
  • The highest complete period was Jun 2026 (297).
  • Sep 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 7,561–7,580 of 17,833 recalls

FDA Recall Completed Historical recordClass II

Walgreens Sodium Chloride Ophthalmic Ointment, 5% Hypertonicity Eye Ointment Sterile, Net Wt. 0.125 oz (3.5 g), Distributed by Walgreen Co. 200 Wilmot Road Deerfield, IL 60015, NDC 0363-7500-50

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Published
November 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Lubricant Eye Drops Moisturizing Twin Pack Walgreens item #: 801477, Package Size: 2 x 15 mL, NDC 0363-0185-49

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Published
November 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Lubricant Eye Drops Moisturizing (Carboxymethycellulose Sodium 0.5% Eye Lubricant), 0.5 oz. (15 mL), Distributed by: Walgreens Co., 200 Wilmot Road, Deerfield, IL 60015, Item #801483

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Published
November 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Puralube Ointment Petrolatum Ophthalmic Ointment, Sterile Ocular Lubricant, Net Wt. 1 g (NDC 0574-4025-11) and Net Wt. 3.5 g (1/8 oz.) (NDC 0574-4025-35), Manufactured for Perrigo, Minneapolis, MN 55427

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Published
November 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Perrigo Sulfacetamide Sodium Ophthalmic Ointment USP, 10% Sterile, Rx only, Net Wt 3.5 g, Manufactured For: Perrigo Minneapolis, MN 55427, NDC 0574-4190-35

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Published
November 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Perrigo Bacitracin Ophthalmic Ointment, Net Wt. 3.5 g (1/8 oz), Rx only, Manufactured For: Perrigo Minneapolis, MN 55427, NDC 0574-4022-35

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Published
November 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Polycin (bacitracin zinc and polymyxin B sulfate) Ophthalmic Ointment USP, Net. Wt. 3.5 g (1/8 oz.), Rx only, Manufactured for Perrigo, Minneapolis, MN 55427, NDC 0574-4021-35

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Published
November 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Perrigo Sterile Neo-Polycin HC (neomycin and polymixin B sulfates, bacitracin zinc and hydrocortisone acetate) Ophthalmic Ointment USP, Net Wt. 3.5 g (1/8 oz), Rx only, Mfd. For Perrigo Minneapolis, MN 55427, NDC 0574-4144-35

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Published
November 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass II

Perrigo Neo-Polycin neomycin and polymixin B sulfates and bacitracin zinc Ophthalmic Ointment Net Wt. 3.5 g, Rx only, Manufactured for Perrigo Minneapolis, MN 55427 NDC 0574-4250-35

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Published
November 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5 mg per 5 mL, 473 mL bottles, Rx only, Mfd. by: KVK-Tech, Inc. Newtown PA 18940; NDC 10702-150-16

by KVK-Tech, Inc.

Reason
Presence of Foreign Substance: Black particles were found in the lots during retain sample inspection
Published
November 20, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Viatrexx-ANS/CNS, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0025, NDC 73069-039-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Viatrexx-Male+, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0400, NDC 73069-320-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Viatrexx-Neuro, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0460, NDC 73069-375-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Viatrexx-Hair, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0251, NDC 73069-206-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Viatrexx-Facial, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0184, NDC 73069-164-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Viatrexx-Intra-Cell, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0280, NDC 73069-250-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Viatrexx-Relief +, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0615, NDC 73069-450-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Viatrexx-Immunexx, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0270, NDC 73069-244-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Viatrexx-Arthros, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0030, NDC 73069-035-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Viatrexx-GI, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0211, NDC 73069-189-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published
November 20, 2019
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.