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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

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

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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

Nystatin Topical Powder, USP, 100,000 USP units per gram, 15 grams per bottle, Rx only, Vensun, NDC 42543-052-61

by X-Gen Pharmaceuticals Inc.

Reason: Presence of Foreign Substance: potential presence of plastic particles.
Published: August 16, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Garden Of Light Inc.

Product: WOODSTOCK ORGANIC MATCHA VANILLA OATS, 1.8 oz (50g) cup UPC…
Reason: Potential for Listeria contamination
Published: August 16, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Coborn's, Inc

Product: Fudge Brownie, Net Wt. 9 oz. (0.6 lb.) (255g), with the foll…
Reason: Some Gluten Free Chocolate Chip Bars were incorrectly labeled as Gluten Free Fudge Brownies. The Gluten Free Chocolate Chip Bars that are incorrectly labeled as Gluten Free Fudge Brownies do contain milk.
Published: August 16, 2017
Distribution: Multiple states

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FDA Recall Terminated Historical recordClass II

Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30

by PD-Rx Pharmaceuticals, Inc.

Reason: Failed Tablet/Capsule Specification: out of specification for tablet weight.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60

by Teva Pharmaceuticals USA

Reason: Failed Tablet/Capsule Specification; out of specification for tablet weight
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets, USP 600 mg, 500-count bottle (Capsule Shaped), Rx only, Manufactured for: Time Cap Labs, Inc., 7 Michael Avenue Farmingdale, NJ 11735, USA, Manufactured by: Marksans Pharma Ltd. Plot No. L-82, L-83 Verna Indl. Estate, Verna, Goa-403 722, India, NDC 49483-603-50

by Time-Cap Laboratories, Inc.

Reason: Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles were found to contain some Ibuprofen Tablets USP 800 mg.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alka-Seltzer Gold (1000 mg Anhydrous citric acid, 344 mg Antacid Potassium bicarbonate, 1050 mg Antacid Sodium bicarbonate/Antacid) Effervescent Tablets, 36-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500041085

by Bayer HealthCare Pharmaceuticals, Inc.

Reason: Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID), 1985 mg Analgesic Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 24-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500044048

by Bayer HealthCare Pharmaceuticals, Inc.

Reason: Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alka-Seltzer Original ( 325 mg Aspirin (NSAID), 1916 mg Analgesic, Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 12-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500040194

by Bayer HealthCare Pharmaceuticals, Inc.

Reason: Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a.) 100-count bottle (NDC 68382-033-01) b.) 500-count bottle (NDC 68382-033-05), Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054

by Zydus Pharmaceuticals USA Inc

Reason: Failed Dissolution Specifications
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Divalproex Sodium Delayed Release Tablets, USP, 250 mg 100-count bottle (NDC 68382-032-01), b.) 500-count bottle (NDC 68382-032-05),Rx only, Manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054

by Zydus Pharmaceuticals USA Inc

Reason: Failed Dissolution Specifications
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Divalproex Sodium Delayed Release Tablets, USP, 125 mg, 100-count bottle Rx only, Manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054, NDC 68382-031-01

by Zydus Pharmaceuticals USA Inc

Reason: Failed Dissolution Specifications
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Albuterol Sulfate Inhalation Solution, 0.021% (0.63 mg/3mL), packaged in 5 pouches of 5 x 3mL Sterile Unit-Dose Vials For Inhalation per carton, Rx only, Mfd. for: Watson Laboratories, Inc., Corona, CA 92880; Mfd. by: Cipla Ltd., Verna, Goa INDIA, NDC 0591-3467-53.

by Teva Pharmaceuticals USA

Reason: Failed Impurities/Degradation Specifications: high out of specification results for related compound D.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Pravastatin Sodium Tablets, USP, 10 mg, packaged in a) 90-count bottles (NDC 55111-229-90) and b) 500-count bottles (NDC 55111-229-05), Rx only, Manufactured by: Dr. Reddy's Laboratories Limited, Bachupally - 500 090 INDIA; Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradation Specifications: high out of specification results for related impurity for lot C700220.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

NatureBox, Inc.

Product: NatureBox Sticks 'n Stones; roasted nuts with sesame sticks.…
Reason: Firm received notification that a consumer found a peanut in NatureBox Sticks 'n Stones snack mix that contains Cashews and Almonds, not peanuts.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Clif Bar & Company

Product: Clif Kid Zbar Protein Chocolate Mint 10-pack, 150-count, 5-…
Reason: Undeclared peanuts and/or tree nuts.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Clif Bar & Company

Product: Clif Kid Zbar Protein Chocolate Chip 10-pack, 150-count, 5-…
Reason: Undeclared peanuts and/or tree nuts.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Clif Bar & Company

Product: Clif Builders Chocolate Mint 12-count, 6-pack, 7-pack, Snac…
Reason: Undeclared peanuts and/or tree nuts.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Clif Bar & Company

Product: Clif Kid Zbar Protein Variety Pack 30-count
Reason: Undeclared peanuts and/or tree nuts.
Published: August 9, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Clif Bar & Company

Product: Clif Builders Variety Pack Chocolate Peanut Butter and Choco…
Reason: Undeclared peanuts and/or tree nuts.
Published: August 9, 2017
Distribution: Nationwide

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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.