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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.

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 4,361–4,380 of 18,222 recalls

FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Similac Water - Sterilized (Export Canada) 2 fl oz reclose…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Similac Stage 1 (Export Dominican Republic) 2 fl oz reclose…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Similac Stage 1 (Export Colombia) 2 fl oz reclose able plast…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Similac Special Care 2 fl oz reclose able plastic bottle Pa…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Similac Total Comfort 2 fl oz reclose able plastic bottle P…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Similac Neosure 2 fl oz reclose able plastic bottle Package…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Similac 360 Total Care Sensitive with Nipples 2 fl oz reclos…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Similac 360 Total Care Sensitive 2 fl oz reclose able plasti…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Similac 360 Total Care/Similac 360 Total Care Sensitive Disc…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Similac 360 Total Care 2 fl oz reclose able plastic bottle…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Pedialyte Unflavored (Export to Canada) 2 fl oz plastic recl…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic r…
Reason
Compromised seal integrity which could lead to spoilage
Published
November 23, 2022
Distribution
Domestic: Alaska, Alabama, Arizona, Cali…

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FDA Recall Terminated Historical recordClass I

Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes, For Subcutaneous or Intravenous Use, Rx Only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505 U.S.A., Made in Italy, NDC: 67457-246-00 (syringe), 67457-246-01 (carton).

by Viatris Inc

Reason
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
Published
November 16, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Hammond's Candies Since 1920 II, LLC

Product
Hammond's Salted Caramel Cookies, NET WT. 5 OZ (142g), UPC 6…
Reason
Peanut Butter Chocolate Chip Cookies mispacked in Salted Caramel Cookies Box creating undeclared peanut allergen.
Published
November 16, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Susvimo (ranibizumab injection), 100mg/mL, sold together as a) carton containing One Susvimo single-dose vial and One Susvimo initial fill needle, NDC 50242-078-55; and b) carton labeled as Susvimo Ocular Implant with Insertion Tool Assembly, containing One carrier with implant and One insertion Tool, UDI 81004259001, GTIN 00810042590014, Rx only, Genentech, Inc., A Member of the Roche Group, South San Francisco, CA 94080-4990.

by Genentech Inc

Reason
Defective Delivery System: Commercial implants do not meet the filed specification for the intended use, a few patients have experienced an issue with the implants that renders it non-functioning.
Published
November 9, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg, 30-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India; NDC 62756-970-83

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Presence of Foreign Substance
Published
November 9, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, Inc. Lehi, Utah 84043, Mfd by: Exela Pharma Sciences, LLC, Lenoir, NC 28645, Carton NDC 72572-740-20, vial NDC 72572-740-1.

by Exela Pharma Sciences LLC

Reason
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx only, Manufactured and Distributed by: Exela Pharma Sciences, LLC Lenoir, NC 28645. Carton NDC 51754-5001-5, vial NDC 51754-5001-1

by Exela Pharma Sciences LLC

Reason
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Quinapril and Hydrochlorothiazide Tablets, USP 20mg/12.5mg, 90 Tablets bottles Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520, Made in India, NDC 65862-162-90

by Aurobindo Pharma USA Inc.

Reason
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Published
November 2, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Atenolol Tablets, USP, 25 mg, 1000-count bottle, Rx only, Manufactured by: ALPHAPHARM PTY LTD, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC 60429-027-10

by Golden State Medical Supply Inc.

Reason
Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets
Published
November 2, 2022
Distribution
Nationwide

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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.