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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.

37,139
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/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 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 11,241–11,260 of 20,777 recalls

FDA Recall Terminated Historical recordClass II

Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye-Free Non-Staining Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by Family Dollar Services, Inc., 10301 Monroe Road, Matthews, NC 28105, NDC 55319-250-23, UPC 0 32251 03374 2.

by Tris Pharma Inc.

Reason
Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Published
December 26, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg per 1.25 mL, Dye-Free Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by Wal-Mart Stores, Inc., Bentonville, AR 72716, NDC 49035-125-23, UPC 0 78742 02016 7.

by Tris Pharma Inc.

Reason
Superpotent Drug: recalled lots may have higher concentration of ibuprofen.
Published
December 26, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Fentanyl Citrate 2 mcg per mL (200 mcg per 100 mL) and Ropivacaine HCl 0.2% in Sodium Chloride 0.9%, Injection, 100 mL total volume in a 150 mL Intravia Bag, Rx Only,PharMEDium Services, LLC. 913 N. Davis Ave. Cleveland, MS 38732. NDC 61553-148-48

by PharMEDium Services, LLC

Reason
Sub-potent
Published
December 26, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Fentanyl Citrate 2 mcg per mL (100 mcg per 50 mL) and Ropivacaine HCl 0.1% in Sodium Chloride 0.9%, Injection, 50 mL total volume in a 60 mL BD Syringe, Rx Only, PharMEDium Services, LLC. 913 N. Davis Ave. Cleveland, MS 38732 NDC 61553-644-75.

by PharMEDium Services, LLC

Reason
Sub-potent
Published
December 26, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Estradiol Tablets, USP, 2 mg, 100-count bottle, Rx Only, Distributed by: Epic Pharma, LLC Laurelton, NY 11413, NDC 42806-089-01

by Epic Pharma, LLC

Reason
Presence of foreign tablet/capsule: A single foreign tablet was found in pharmacy dispensed bottle of 30 Estradiol 2 mg tablets.
Published
December 26, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC

Product
Inspired Organic Peanut Butter 16oz. plastic jar, 6 per cas…
Reason
Product testing returned positive test results for Listeria monocytogenes.
Published
December 26, 2018
Distribution
FL, IA, IL, IN, KY, MD, MI, MN, MO, NY,…

View recall →

FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC

Product
Inspired Organic Tahini Butter 16oz. plastic jar, 6 per cas…
Reason
Product testing returned positive test results for Listeria monocytogenes.
Published
December 26, 2018
Distribution
FL, IA, IL, IN, KY, MD, MI, MN, MO, NY,…

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FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC

Product
Inspired Organic Almond Butter 16oz. plastic jar, 6 per cas…
Reason
Product testing returned positive test results for Listeria monocytogenes.
Published
December 26, 2018
Distribution
FL, IA, IL, IN, KY, MD, MI, MN, MO, NY,…

View recall →

FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC

Product
Inspired Organic Sunflower Butter 16oz. plastic jar, 6 per…
Reason
Product testing returned positive test results for Listeria monocytogenes.
Published
December 26, 2018
Distribution
FL, IA, IL, IN, KY, MD, MI, MN, MO, NY,…

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FDA Recall United States Terminated Historical recordClass I

DANONE WATERS OF AMERICA INC

Product
LIGHT & FIT¿ GREEK CRUNCH NONFAT YOGURT & TOPPINGS S MORES F…
Reason
Danone North America is voluntarily recalling Light & Fit¿ Greek Crunch Nonfat Yogurt & Toppings S Mores Flavor because it was discovered that some of the toppers sold on the product contain peanuts and are improperly labeled.
Published
December 26, 2018
Distribution
13 states: Connecticut, Illinois, Iowa,…

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FDA Recall United States Terminated Historical recordClass I

Kwik Trip, Inc.

Product
Kitchen Cravings Strawberry Parfait, Net Wt 8.25 oz (234g)…
Reason
Kitchen Cravings Strawberry and Mixed Berry Parfaits in an 8.25 oz. cup may contain undeclared traces of tree nuts(specifically almond and cashew).
Published
December 26, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Kwik Trip, Inc.

Product
Kitchen Cravings Mixed Berry Parfait, Net Wt 8.25 oz (234g)…
Reason
Kitchen Cravings Strawberry and Mixed Berry Parfaits in an 8.25 oz. cup may contain undeclared traces of tree nuts(specifically almond and cashew).
Published
December 26, 2018
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass I

Country Favor Inc.

Product
Best Taste Brand DRIED BAMBOO SHOOT Mang Non. The product co…
Reason
Product contains undeclared sulfites (75 mg per serving).
Published
December 26, 2018
Distribution
AL, AR , FL, GA, IL,KY, LA, MA, MD,MI,MO…

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FDA Recall United States Terminated Historical recordClass I

Oakhouse Bakery

Product
Kwik Trip Granola, Bulk Granola, 09976. Net Wt 20 lbs / 9.1…
Reason
Bulk Granola may contain undeclared tree nuts (specifically cashew and almond)
Published
December 26, 2018
Distribution
WI only

View recall →

FDA Recall United States Terminated Historical recordClass I

Marich Confectionery Company, Inc.

Product
Milk Chocolate Maltballs: NET Wt. 15 lbs. Item number 992…
Reason
Firm was notified by a direct customer that milk chocolate macadamia nuts were found in their shipment of milk chocolate maltballs.
Published
December 26, 2018
Distribution
CA, CO, HI, ID, IL, IN, KS, MA, MI, MN.…

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FDA Recall Ongoing Historical recordClass II

Amlodipine, Valsartan, and Hydrochlorothiazide Tablets 10 mg/320 mg/25 mg, (a) 30-count bottles (NDC 0093-7809-56) & 90-count bottles (NDC 0093-7809-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Amlodipine, Valsartan, and Hydrochlorothiazide Tablets 10 mg/160 mg/25 mg, (a) 30-count bottles (NDC 0093-7960-56) & 90-count bottles (NDC 0093-7690-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Amlodipine, Valsartan, and Hydrochlorothiazide Tablets 10 mg/160 mg/12.5 mg, (a) 30-count bottles (NDC 0093-7810-56) & 90-count bottles (NDC 0093-7810-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Amlodipine, Valsartan, and Hydrochlorothiazide Tablets 5 mg/160 mg/12.5 mg, (a) 30-count bottles (NDC 0093-7807-56) & 90-count bottles (NDC 0093-7807-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Amlodipine and Valsartan Tablets 10 mg/320 mg (a) 30-count bottles (NDC 0093-7693-56) & 90-count bottles (NDC 0093-7693-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
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.