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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 11,841–11,860 of 20,954 recalls

FDA Recall Terminated Historical recordClass II

Fluticasone propionate Nasal Spray, USP, 50 mcg, packaged in 50 mcg per spray 120 Metered Sprays bottles, 16 g net fill weight, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, FL 33326, NDC 60505-0829-1

by Apotex Inc.

Reason
Presence of foreign substance: glass particles
Published
June 13, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Dean Foods, Inc.

Product
Baskin Robbins Mint Chocolate Chip
Reason
Product may contain unlabeled coconut.
Published
June 13, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Lake Michigan Distilling Co LLC

Product
Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, M…
Reason
Lake Michigan Distilling, LLC, dba Ethanol Extraction has initiated a voluntary recall of Ethanol Extraction s 190 Proof Non-Denatured Grain Alcohol due to contamination with methanol which could cause serious injury or death if consumed.
Published
June 13, 2018
Distribution
Domestic: AK, AL, AR, AZ, CA, CO, CT, DC…

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FDA Recall Terminated Historical recordClass I

7K capsules packaged in single packs sold in 24-count boxes, Distributed by SX Power Co. San Diego, CA 92108, UPC 601577513148

by Shoreside Enterprises Inc.

Reason
Marketed Without An Approved NDA/ANDA: FDA analysis found products to contain undeclared sildenafil and tadalafil. The presence of sildenafil and tadalafil makes these products an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Published
June 6, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857

by Shoreside Enterprises Inc.

Reason
Marketed Without An Approved NDA/ANDA: FDA analysis found products to contain undeclared sildenafil and tadalafil. The presence of sildenafil and tadalafil makes these products an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Published
June 6, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

JJBL LLC

Product
The Most Awesome Chocolate Bar EVER, packaged individually i…
Reason
The Most Awesome Chocolate Bar EVER is recalled due to undeclared wheat.
Published
June 6, 2018
Distribution
Distributed in CA, OR, and WA.

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FDA Recall United States Terminated Historical recordClass II

Ohio Hickory Harvest Brand Products Inc.

Product
Liberty Snacks NUTS ALMOND RAISIN Mix Net Wt. 1.6 oz (#g) DI…
Reason
The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
Published
June 6, 2018
Distribution
Product was only distributed in the foll…

View recall →

FDA Recall United States Terminated Historical recordClass II

Ohio Hickory Harvest Brand Products Inc.

Product
Liberty Snacks Raw ALMONDS Net Wt. 1.3 oz (#g) DISTRIBUTED B…
Reason
The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
Published
June 6, 2018
Distribution
Product was only distributed in the foll…

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FDA Recall United States Terminated Historical recordClass II

Ohio Hickory Harvest Brand Products Inc.

Product
Liberty Snacks Honey Roasted CASHEWS Net Wt. 1.2 oz (#g) DIS…
Reason
The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
Published
June 6, 2018
Distribution
Product was only distributed in the foll…

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FDA Recall United States Terminated Historical recordClass II

Ohio Hickory Harvest Brand Products Inc.

Product
Liberty Snacks Natural PISTACHIOS Net Wt. 1 oz (#g) DISTRIBU…
Reason
The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
Published
June 6, 2018
Distribution
Product was only distributed in the foll…

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FDA Recall United States Terminated Historical recordClass II

Ohio Hickory Harvest Brand Products Inc.

Product
Hickory Harvest Island Fruit Mix NET WT 9 oz (255g) Distribu…
Reason
The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
Published
June 6, 2018
Distribution
Product was only distributed in the foll…

View recall →

FDA Recall United States Terminated Historical recordClass II

Ohio Hickory Harvest Brand Products Inc.

Product
Heinens Organic Nut Mix Net Wt. 9 oz (255g) Distributed By H…
Reason
The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.
Published
June 6, 2018
Distribution
Product was only distributed in the foll…

View recall →

FDA Recall Terminated Historical recordClass II

My Way (levonorgestrel) Tablets TWO PACK, 1.5 mg each, packaged as 2 Treatments (Two 1.5mg Levonorgestrel Tablets) per carton, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202; Manufactured by: Lupin Limited, Pithampur (M.P.) - 454 775, INDIA, UPC 3 68180 85212 4.

by Lupin Pharmaceuticals Inc.

Reason
Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive appropriate regulatory approval prior to release.
Published
May 30, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

My Way (Levonorgestrel) Tablets TWO PACK, 1.5 mg each, packaged as 2 Treatments (Two 1.5mg Levonorgestrel Tablets) per carton, GAVIS Pharmaceuticals, A Lupin Group Company; Mfg. for Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, UPC 3 43386-622-31 3.

by Lupin Pharmaceuticals Inc.

Reason
Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive appropriate regulatory approval prior to release.
Published
May 30, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

screamin' menthol (menthol) Pain Relieving Gel, 4%, packaged in a) 2 OZ (57g) tubes, UPC 7 50263 80062 5; b) 5 oz. (141g) tubes, UPC 7 50263 80006 9; and c) 16 oz. (454g) bottles, UPC 7 50263 80066 3; MFD FOR: Toast Products, 400 Sproul Street, Pittsburgh, PA 15136; NDC 52099-8010.

by Ideaz Llc

Reason
CGMP Deviations: Products manufactured with an ingredient that exceed the benzene levels allowed in drug products.
Published
May 30, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Diclofenac Sodium and Misoprostol Delayed Release Tablets 75 mg/0.2 mg, 60-count bottle, Rx Only, Manufactured by: Cipla Ltd., India; For: EAGLE PHARMACEUTICALS, INC., Woodcliff Lake, NJ 07677 USA, NDC 42367-111-06.

by Exela Pharma Sciences LLC

Reason
Labeling: Label Mix-Up: bottle labeled as Diclofenac Sodium and Misoprostol 75 mg/0.2 mg contained Diclofenac Sodium and Misoprostol 50 mg/0.2 mg tablets.
Published
May 30, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Loxapine Capsules, USP 50 mg, packaged in 100 Unit Dose capsules, Rx only, Manufactured by Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. NDC 51079-903-20.

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason
GMP Deviations: a recent FDA inspection of the manufacturing site revealed multiple cGMP violations that would place Loxapine at risk for cross contamination
Published
May 30, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Loxapine Capsules, USP 25 mg, packaged in 100 Unit Dose Capsules, Rx only, Manufactured by Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. NDC 51079-902-20

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason
GMP Deviations: a recent FDA inspection of the manufacturing site revealed multiple cGMP violations that would place Loxapine at risk for cross contamination
Published
May 30, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack, Distributed by AMA Wholesale Inc. Chino Hills, CA, 91709-2618, UPC Code: 718122071128

by AMA Wholesale

Reason
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared tadalafil. The presence of tadalafil makes Rhino Extreme 50000 an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Published
May 30, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

screamin' hot (capsaicin) Pain Relieving Gel, 0.03%, packaged in a) 2 OZ (57g) tubes, UPC 7 50263 80072 4; b) 5 oz. (141g) tubes, UPC 7 50263 80007 6; and c) 16 oz. (454g) bottles, UPC 7 50263 80076 2; MFD FOR: Toast Products, 400 Sproul Street, Pittsburgh, PA 15136; NDC 52099-8005.

by Ideaz Llc

Reason
CGMP Deviations: Products manufactured with an ingredient that exceed the benzene levels allowed in drug products.
Published
May 30, 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.