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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.

37,324
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,859
Class I recallsReasonable probability of serious health consequences
24,440
Class II recallsTemporary or medically reversible health consequences
2,900
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 2,095 recalls
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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • 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 II24,440
Class I9,859
Class III2,900
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,440
Class I9,859
Class III2,900
Not Yet Classified2

Showing 4,621–4,640 of 19,481 recalls

FDA Recall United States TerminatedTerminated: February 14, 2023Historical recordClass I

Whole Foods Market Brand 365, Llc

Product
Whole Foods Market Dipping Caramel, PLU 34888 sold by the po…
Reason
Undeclared wheat
Published
November 16, 2022
Distribution
NE, CO, and KS

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FDA Recall United States TerminatedTerminated: January 11, 2024Historical 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 United States TerminatedTerminated: December 13, 2022Historical recordClass II

Taylor Farms Retail, Inc.

Product
BabyBel Snacker (FG0401 SW Snacker ACABB 5pk) Crunch Pak 5.7…
Reason
Allergens of almonds and milk not declared on the product ingredient label
Published
November 16, 2022
Distribution
Product was distributed to consignees lo…

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FDA Recall TerminatedTerminated: April 17, 2024Historical 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 TerminatedTerminated: September 7, 2023Historical 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 United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Lactaid Cottage Cheese, 16 oz
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Hood Lowfat Cottage Cheese with Peaches
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Hood Lowfat Cottage Cheese, 16 oz and 24 oz
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Hood Fat Free Cottage Cheese with Pineapple, 16 oz
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Hood Everything Bagel Cottage Cheese, 16 oz
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Hood Cottage Cheese with Strawberries; 16 oz
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Hood Cottage Cheese with Pineapple & Cherry, 16 oz; Penn Mai…
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Hood Cottage Cheese with Cucumber & Dill, 16 oz
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Hood Cottage Cheese with Blueberries, 16 oz
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Hannaford Fat Free Cottage Cheese, 16 oz and 24 oz; Hood Fat…
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Food Club Cottage Cheese with Pineapple, 16 oz; Hannaford Co…
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Hannaford Cottage Cheese, 16oz and 24 oz; Hood Country Style…
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall United States TerminatedTerminated: March 1, 2023Historical recordClass II

HP Hood LLC

Product
Food Club Chive Cottage Cheese, 16 oz; Hannaford Chive Cotta…
Reason
Product may contain foreign objects (plastic).
Published
November 9, 2022
Distribution
Alabama, Arizona, California, Colorado,…

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FDA Recall TerminatedTerminated: October 10, 2025Historical 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 TerminatedTerminated: October 10, 2025Historical 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

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.

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