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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
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 13,361–13,380 of 21,635 recalls

FDA Recall Terminated Historical recordClass II

All sterile drug preparations remaining within expiry prepared from Fentanyl Citrate Base Solution dispensed between October 16, 2017 and November 17, 2017 Compounded by Intrathecal Compounding Specialists, Scott, LA 70583.

by Intrathecal Compounding Specialist, LLC

Reason
Lack of sterility assurance.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Ciclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15); b) 30 g tubes (NDC 0713-0638-31); and c) 90 g tubes (NDC 0713-0638-18), Rx Only, Manufactured by: G&W Laboratories, Inc., South Plainfield, NJ 07080.

by G & W Laboratories, Inc.

Reason
Discoloration: Product is supposed to be a white to off white homogenous cream and may have intermittent yellow discoloration.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product
Reduced-Fat Wild Blueberry Cream Cheese, 2 oz. and 8 oz.
Reason
Product may be contaminated with Listeria monocytogenes.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product
Panera Reduced-Fat Honey Walnut Cream Cheese, 2 oz. and 8 oz…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product
Panera Chive&Onion Reduced Fat Cream Cheese Spread, 2 oz. an…
Reason
Product may be contaminated with Listeria monocytogenes.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods Llc

Product
SunGlow, European Style Butter Blend Margarine, packaged in…
Reason
SunGlow contains undeclared soy lecithin.
Published
February 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods Llc

Product
SunGlow, Unsalted European Style Butter Blend Margarine (169…
Reason
SunGlow contains undeclared soy lecithin.
Published
February 14, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Mountain Rose Inc

Product
Prickly Ash Bark Powder Herbal Supplement, packaged in food…
Reason
Prickly Ash Bark Powder is recalled due to a potential contamination with Salmonella.
Published
February 14, 2018
Distribution
distributed in AK, AR, AZ, CA, CO , FL,…

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FDA Recall United States Terminated Historical recordClass II

Simply Delicious, Inc. dba Bobo's Oat Bars

Product
Bobo's Coconut Oat Bar 3oz. Packaged in overwrap film per…
Reason
Bobo's recalled Coconut 3oz Bar due to mold.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product
Panera Reduced-Fat Plain Cream Cheese, 2 oz. and 8 oz.
Reason
Product may be contaminated with Listeria monocytogenes.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Panera, LLC

Product
Panera Plain Cream Cheese, 2 oz. and 8 oz.
Reason
Product may be contaminated with Listeria monocytogenes.
Published
February 14, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

J F C International Inc

Product
Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per…
Reason
Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.
Published
February 14, 2018
Distribution
CA, NV, WA, OR, UT, AK, AZ, TX, OK, OH,…

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FDA Recall United States Terminated Historical recordClass II

CHOBANI

Product
Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogur…
Reason
Product is recalled because a statement on the overwrap label erroneously states "No Gluten" while the ingredients statement and the Contains statements on both the overwrap label and the flip label on each individual cup declare wheat.
Published
February 14, 2018
Distribution
distributed in AL, AR, AZ, CA, CO, CT,…

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FDA Recall Terminated Historical recordClass I

Nexterone (amiodarone HCl) Premixed Injection, 150mg/100mL, 100-mL bag, Rx Only, Sterile, Baxter Healthcare Corporation, Deerfield, IL. NDC 43066-150-10

by Baxter Healthcare Corporation

Reason
Presence of Particulate Matter:Particulate identified as polyethylene, the primary constituent of the film and ports used to manufacture the bag in which product is packaged
Published
February 7, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Tiger King tablets, labeling is in foreign language

by A&H Focal Inc.

Reason
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.
Published
February 7, 2018
Distribution
NY and NJ through six retail stores name…

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FDA Recall Terminated Historical recordClass I

MACA gold tablets, 6800 mg, 10-count bottle, labeling is in foreign language

by A&H Focal Inc.

Reason
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.
Published
February 7, 2018
Distribution
NY and NJ through six retail stores name…

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FDA Recall Terminated Historical recordClass I

LIEN CHAN FOR SEVEN DAYS capsules, labeling is in foreign language

by A&H Focal Inc.

Reason
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.
Published
February 7, 2018
Distribution
NY and NJ through six retail stores name…

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FDA Recall Terminated Historical recordClass I

DADIYONGSHI XIANGGANGTIANLONGSHENGWU tablets, 6-count bottle, labeling is in foreign language

by A&H Focal Inc.

Reason
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.
Published
February 7, 2018
Distribution
NY and NJ through six retail stores name…

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FDA Recall Terminated Historical recordClass I

Power V8 Viagra tablets, 200mg, 10-Grain bottle, labeling is in foreign language

by A&H Focal Inc.

Reason
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.
Published
February 7, 2018
Distribution
NY and NJ through six retail stores name…

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FDA Recall Terminated Historical recordClass I

YANSHIJIAONANG capsules, 2000mg, 8-count bottle, labeling is in foreign language

by A&H Focal Inc.

Reason
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.
Published
February 7, 2018
Distribution
NY and NJ through six retail stores name…

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.