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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.

37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,241–12,260 of 18,488 recalls

FDA Recall United States Terminated Historical recordClass I

Bulletproof 360 Inc

Product
Fudge Brownie Collagen Protein Bar. Each bar is packed in f…
Reason
Fudge Brownie Collagen Protein Bar product is recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Unilever United States, Inc.

Product
Ben & Jerry's Pint Slices Chocolate Fudge Brownie 3 chocol…
Reason
Unilever is voluntarily recalling a limited number of boxes of Ben & Jerry's Chocolate Fudge Brownie Pint Slices due to undeclared peanut.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Nutri-Dyn Midwest, Inc.

Product
Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 C…
Reason
During production of St. John's Wort, Lot 160876, a number of bottles were mistakenly labeled as Calcium D-Glucarate Plus
Published
July 12, 2017
Distribution
US: AZ, CA, CO,, FL, IA, ID, MA, MD, MI,…

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FDA Recall United States Terminated Historical recordClass II

GoMacro, Inc.

Product
go macro THRIVE Caramel Coconut bar, Net Wt 1.4 oz / 40 G, U…
Reason
GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

GoMacro, Inc.

Product
go macro THRIVE Chocolate, Nuts & Sea Salt bar, Net Wt 1.4 o…
Reason
GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.
Published
July 12, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

GoMacro, Inc.

Product
go macro MACROBAR, coconut + almond butter + chocolate chips…
Reason
GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.
Published
July 12, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Bolner's Fiesta Products, Inc

Product
Chili Pequino 0.25 oz packaged in a clear plastic bag; Produ…
Reason
Low levels of peanuts detected
Published
July 12, 2017
Distribution
US. AR, AZ, CO, GA, ID, KS, LA, MI, MO,…

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FDA Recall Terminated Historical recordClass II

Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10%/0.2% sterile, 3.5 g tube, RX only, Manufactured by Allergan, Irvine, California, 92612, U.S.A., NDC: 0023-0313-04.

by Allergan Sales, LLC

Reason
Failed Impurities/Degradation Specifications: stability testing results did not meet the specification for impurities.
Published
July 5, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center, Suite 400, Princeton, NJ 08805, NDC: 63739-706-10

by Mckesson Packaging Services

Reason
Failed Moisture Limits: Product tested out-of-specification for moisture content.
Published
July 5, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Doxycycline Hyclate USP, active pharmaceutical ingredient, a) 25 g packaged in a 500 cc container (NDC: 58597-8082-4), b) 100 g packaged in 16 oz container (NDC: 58597-8082-6), c) 500 g packaged in a 2500 cc container (NDC: 58597-8082-7) and a 1,000 g packaged in 1 gallon container (NDC: 58597-8082-8). For Prescription Compounding RX Only. Packed under cGMP conditions by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327

by American Pharmaceutical Ingredients LLC

Reason
Labeling: Not Elsewhere Classified. Manufacturer and product were discovered to be on FDA Import Alert 66-66 for misbranding of active pharmaceutical ingredient.
Published
July 5, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor Chewable Tablets, 80 mg & 14.2 mg, 100-count bottles, Distributed by: GlaxoSmithKline Consumer Healthcare, L.P., Moon Twp, PA 15108, UPC 3 0088-1175-47 8.

by Sanofi-Aventis U.S. LLC

Reason
Superpotent Drug: high out-of-specification result for magnesium.
Published
July 5, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Progesterone Injection in Olive Oil With Benzyl Alcohol 10%, 50mg/mL, 10mL Multi-Dose Vial, Rx only, Apothecary by Design, 141 Preble Street, Portland, ME.

by Apothecary By Design

Reason
Lack of Processing Controls: The metal container closure adheres to the rubber stopper on some of the units of the batch which can impact the integrity of the container closure.
Published
July 5, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Minivelle (estradiol Transdermal System) 0.1 mg per day, pack of 8 systems per carton, Rx only, Dist. by: Noven Therapeutics, LLC. Miami, Florida 33186. NDC: 68968-6610-8

by Noven Pharmaceuticals, Inc.

Reason
Defective Delivery System: Out of specification for peel force from the release liner specification during stability testing at 18M 25C/60%RH.
Published
July 5, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Magnesium Citrate Saline Laxative Cherry Flavored, packaged in a) 10 fl. oz. (296 mL) bottle UPC: 072785104556 (Rexall's label), b) 10 fl. oz. (296 mL) bottle UPC: 041163254138 (Equaline's label), OTC, Distributed by a) Dolgencorp, LL, Goodlettsville, TN 37072 b)Supervalu, Inc. Eden Prairie, MN 55344

by Vi-Jon, Inc.

Reason
Presence of foreign substance: glass particle
Published
June 28, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.

by Lucid Pharma LLC

Reason
Failed Tablet/Capsules Specifications: pharmacists complaints for bottles containing melted capsules.
Published
June 28, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Monfitello

Product
Private Selection Peruvian Inspired Aji Amarillo Culinary Sp…
Reason
The firm was notified that the product may contain peanuts.
Published
June 28, 2017
Distribution
Products were shipped to the following s…

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FDA Recall United States Terminated Historical recordClass I

Monfitello

Product
PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINA…
Reason
The firm was notified that the product may contain peanuts.
Published
June 28, 2017
Distribution
Products were shipped to the following s…

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FDA Recall Terminated Historical recordClass III

Montelukast Sodium Oral Granules, 4 mg pouch, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-6040-93

by Mylan Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications; out of specification results for Sulphoxide Impurity and Total Impurities
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Human Chorionic Gonadotropin, 15,000 IU per vial, lyophilized for injection, Rx only, Complete Pharmacy & Medical Solutions, Miami Lakes, FL 33014

by Complete Pharmacy and Medical Solutions LLC

Reason
Non-sterility - presence of bacteria confirmed by outside laboratory after day 14.
Published
June 21, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

VANCOMYCIN HCl 1.5g in 300 mL 5% Dextrose Injection USP, Service Code 2K2227, NDC# 61553-027-34, Total Volume 300.00 mL incorrectly labeled as 500.00 mL, Rx Only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 74478

by PharMEDium Services, LLC

Reason
Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.
Published
June 21, 2017
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.