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Recall totals

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

37,135

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

State: MP ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 23, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass III

Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-25

by Pharmedium Services Llc

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date
Published: July 12, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-03

by Pharmedium Services Llc

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date
Published: July 12, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Ropivacaine HCl 0.2% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-256-09

by Pharmedium Services Llc

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date
Published: July 12, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Bulletproof 360 Inc

Product: Vanilla Shortbread Collagen Protein Bite. Each Bite is packe…
Reason: Vanilla Shortbread Collagen Protein Bite 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 I

Bulletproof 360 Inc

Product: Vanilla Shortbread Collagen Protein Bar. Each Bar is packed…
Reason: Vanilla Shortbread 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 I

Bulletproof 360 Inc

Product: Lemon Cookie Collagen Protein Bar. Each Bar is packed in fo…
Reason: Lemon Cookie 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 I

Bulletproof 360 Inc

Product: Fudge Brownie Collagen Protein Bite. Each Bite is packed in…
Reason: Fudge Brownie Collagen Protein Bite 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 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

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

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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 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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Data last updated: September 23, 2026 ET

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.