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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

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

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Source: FDA and USDA public dataLast updated September 25, 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

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 II

Clindamycin Injection USP; 600 mg/4 mL (150 mg/mL). 4 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for Alvogen, Inc., Pine Brook, NJ 07058, NDC 47781-463-69

by Alvogen, Inc

Reason: Lack of Assurance of Sterility
Published: July 12, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clindamycin Injection USP; 300 mg/2 mL (150 mg/mL). 2 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for Alvogen, Inc., Pine Brook, NJ 07058, NDC 47781-462-69

by Alvogen, Inc

Reason: Lack of Assurance of Sterility
Published: July 12, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000 g container (NDC: 58597-8023-8). 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: CGMP Deviations: Lack of quality assurance at the API manufacturer.
Published: July 12, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Bupivacaine HCl 0.25% 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: 61553-023-09

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 Terminated Historical recordClass III

Bupivacaine HCl 0.25% 270 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 270 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-044-57

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% 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

View recall →

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

View recall →

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

View recall →

Data last updated: September 25, 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.