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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,113

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 15, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/10 mg, a) 90 count (NDC 43598-742-90) and b) 1000 count (NDC 43598-742-10) bottles, Rx only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA, , packaged in bottles.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Published: November 10, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ivar's Commissary

Product: Ivar's Kettle Classic Clam Chowder With Uncured Bacon, Item…
Reason: Plastic fragments.
Published: November 10, 2021
Distribution: distributed in Illinois, Indiana, Iowa,…

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FDA Recall United States Terminated Historical recordClass I

POTANDON PRODUCE LLC

Product: Green Giant Fresh whole RED onions in 2 lbs. flexible mesh b…
Reason: Potential to be contaminated with Salmonella Oranienburg.
Published: November 10, 2021
Distribution: Distributed in ND and MN.

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FDA Recall United States Terminated Historical recordClass I

POTANDON PRODUCE LLC

Product: Green Giant Fresh whole WHITE onions in 2 lbs. flexible mesh…
Reason: Potential to be contaminated with Salmonella Oranienburg.
Published: November 10, 2021
Distribution: Distributed in ND and MN.

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FDA Recall United States Terminated Historical recordClass I

POTANDON PRODUCE LLC

Product: Green Giant Fresh whole YELLOW onions in 2 lbs. flexible mes…
Reason: Potential to be contaminated with Salmonella Oranienburg.
Published: November 10, 2021
Distribution: Distributed in ND and MN.

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FDA Recall United States Terminated Historical recordClass II

NSE Products, Inc.

Product: Pharmanex Kids Jungamals, Dietary Supplement 90 Chewable Tab…
Reason: Pharmanex Jungamals was found to have a missing fish allergen statement on the label due to fish gelatin as a sub-component of the Vitamin E ingredient.
Published: November 10, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pepsico Inc

Product: Starbucks Doubleshot Espresso, Espresso & Salted Caramel Cre…
Reason: An issue with adequate sealing of canned coffee products potentially lead to premature spoilage.
Published: November 10, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pepsico Inc

Product: Starbucks Doubleshot Espresso, Espresso & Light Cream, 6.5 F…
Reason: An issue with adequate sealing of canned coffee products potentially lead to premature spoilage.
Published: November 10, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pepsico Inc

Product: Starbucks Doubleshot Espresso, Espresso & Cream, 6.5 FL OZ U…
Reason: An issue with adequate sealing of canned coffee products potentially lead to premature spoilage.
Published: November 10, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Kansas City LLC., DBA Best Harvest Bakeries

Product: Hotdog buns, in unlabeled clear plastic bags, 30 or 12 buns…
Reason: Positive environmental samples analyzed for Listeria and Salmonella species.
Published: November 10, 2021
Distribution: Distributed to restaurants in AR, CO, IA…

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FDA Recall United States Terminated Historical recordClass II

Kansas City LLC., DBA Best Harvest Bakeries

Product: Potato buns, in unlabeled clear plastic bags, 30 or 12 buns…
Reason: Positive environmental samples analyzed for Listeria and Salmonella species.
Published: November 10, 2021
Distribution: Distributed to restaurants in AR, CO, IA…

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FDA Recall United States Terminated Historical recordClass II

Kansas City LLC., DBA Best Harvest Bakeries

Product: Hamburger buns, 5" in unlabeled clear plastic bags, 30 or 12…
Reason: Positive environmental samples analyzed for Listeria and Salmonella species.
Published: November 10, 2021
Distribution: Distributed to restaurants in AR, CO, IA…

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FDA Recall United States Terminated Historical recordClass II

Kansas City LLC., DBA Best Harvest Bakeries

Product: Hamburger buns, 4.5" in unlabeled clear plastic bags, 30 or…
Reason: Positive environmental samples analyzed for Listeria and Salmonella species.
Published: November 10, 2021
Distribution: Distributed to restaurants in AR, CO, IA…

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FDA Recall United States Terminated Historical recordClass II

Kansas City LLC., DBA Best Harvest Bakeries

Product: Hamburger buns, 4" in unlabeled clear plastic bags, 30 or 12…
Reason: Positive environmental samples analyzed for Listeria and Salmonella species.
Published: November 10, 2021
Distribution: Distributed to restaurants in AR, CO, IA…

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FDA Recall United States Terminated Historical recordClass II

Kansas City LLC., DBA Best Harvest Bakeries

Product: Hotdog buns, customer specified formula, in unlabeled clear…
Reason: Positive environmental samples analyzed for Listeria and Salmonella species.
Published: November 10, 2021
Distribution: Distributed to restaurants in AR, CO, IA…

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FDA Recall United States Terminated Historical recordClass II

Kansas City LLC., DBA Best Harvest Bakeries

Product: Hamburger buns, customer specified formula, in unlabeled cle…
Reason: Positive environmental samples analyzed for Listeria and Salmonella species.
Published: November 10, 2021
Distribution: Distributed to restaurants in AR, CO, IA…

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FDA Recall Terminated Historical recordClass III

Gatifloxacin Ophthalmic Solution, 0.5%, 2.5 mL bottle, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, INDIA, NDC 68180-435-01.

by Lupin Pharmaceuticals Inc.

Reason: Failed Stability Specifications: Out-of-specification results observed in a water loss test that might affect the assay content and alter drug concentration.
Published: November 3, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Rizatriptan Benzoate Orally Disintegrating Tablets 10mg, 18 Tablets (3 x 6 Unit-Dose Tablets) Blister Packs, Rx only, Manufactured for: Macleods Pharma USA Inc. Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, INDIA, NDC 33342-094-41

by MACLEODS PHARMA USA, INC

Reason: Out-of-specification test results obtained in Organic Impurities test during analysis of controlled samples.
Published: November 3, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Rizatriptan Benzoate Orally Disintegrating Tablets 5mg, 12 Tablets (2 x 6 Unit-Dose Tablets) Blister Packs, Rx only, Manufactured for: Macleods Pharma USA Inc. Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, INDIA, NDC 33342-093-41

by MACLEODS PHARMA USA, INC

Reason: Out-of-specification test results obtained in Organic Impurities test during analysis of controlled samples.
Published: November 3, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Rizatriptan Benzoate Film Coated Tablets, 10 mg, packaged in a) 12 Tablets (2X6 Unit-Dose Tablets) Blister Packs, NDC 33342-088-45), b) 18 Tablets (3 x 6 Unit-Dose Tablets, NDC 33342-088-41) Rx only, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536l Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, INDIA

by MACLEODS PHARMA USA, INC

Reason: Out-of-specification test results obtained in Organic Impurities test during analysis of controlled samples.
Published: November 3, 2021
Distribution: Nationwide

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Data last updated: September 15, 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.