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Recall totals

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

37,204

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 30, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall Terminated Historical recordClass III

Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Pump in 0.9% Sodium Chloride Injection, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-100-13

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% 750 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 600 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-279-33

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: 61553-258-25

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 II

Slade Gorton & Company, Inc.

Product: Gourmet Bay - Honey Mustard Breaded Tilapia, 5-7 oz.. refrig…
Reason: Products recalled due to undeclared allergen -milk
Published: July 12, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Slade Gorton & Company, Inc.

Product: Gourmet Bay - Citrus Coconut Breaded Tilapia, 5-7 oz (Bulk 5…
Reason: Products recalled due to undeclared allergen -milk
Published: July 12, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Slade Gorton & Company, Inc.

Product: Gourmet Bay - Toasted Crumb Breaded Tilapia, 5-7 oz. (Bulk…
Reason: Products recalled due to undeclared allergen -milk
Published: July 12, 2017
Distribution: Multiple states

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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

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

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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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Data last updated: September 30, 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.