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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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: AK ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 13, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

Doxycycline (as Calcium) (equivalent to 50mg/5mL), 10 mg/ml, 60 ml suspension bottles, Peppermint, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Dr, Ste 200, Swedesboro, NJ 08085

by Wedgewood Village Pharmacy, LLC

Reason: Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bethanechol Chloride 1mg/ml, 80 ml Suspension bottles Banana/Strawberry, Qty:1, Wedgewood Village Pharmacy LLC, 405 Heron Dr. Ste 200, Swedesboro, NJ 08085

by Wedgewood Village Pharmacy, LLC

Reason: Lack of Processing Controls: Insanitary conditions observed during recent FDA Inspection
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Enalapril Maleate Tablets, USP; 20 mg; 90 tablets, NDC 60429-186-90; manufactured by Taro Pharmaceutical Industries, Ltd.; packaged by GSMS, Incorporated, CA.

by Golden State Medical Supply Inc.

Reason: CGMP Deviations
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Enalapril Maleate Tablets, USP; 10 mg; 90 tablets, NDC 60429-185-90; manufactured by Taro Pharmaceutical Industries, Ltd.; packaged by GSMS, Incorporated, CA.

by Golden State Medical Supply Inc.

Reason: CGMP Deviations
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Enalapril Maleate Tablets, USP; 5 mg; 90 tablets, NDC 60429-184-90; manufactured by Taro Pharmaceutical Industries, Ltd.; packaged by GSMS, Incorporated, CA.

by Golden State Medical Supply Inc.

Reason: CGMP Deviations
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Enalapril Maleate Tablets, USP; 2.5 mg; 90 tablets, NDC 60429-183-90; manufactured by Taro Pharmaceutical Industries, Ltd.; packaged by GSMS, Incorporated, CA, USA.

by Golden State Medical Supply Inc.

Reason: CGMP Deviations
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate Injection, USP, 200mg/ml, Rx Only, One Single-dose vial, Distributed by: Sun Pharmaceutical Industries Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceuticals Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-015-40.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: CGMP Deviations: Manufacturing deviations were reported due to an abnormal appearance on parts of machinery.
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

CVS Health Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Lemon Flavor, 10 FL OZ (296 mL), Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 30594 2.

by Vi-Jon, LLC

Reason: Microbial Contamination of a Non-Sterile Products: Testing of product onfirmed the presence of Gluconacetobacter Liquefaciens
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Eszopiclone Tablets, USP 1 mg, packaged in 30-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd., Baddi, Himachal Pradesh, INDIA, NDC 33342-299-07

by Macleods Pharma Usa Inc

Reason: Shortfill: customer complaints of one to three tablets were reported missing from 30 count bottles.
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Mometasone Furoate, Topical Solution USP, 0.1 % Lotion, a) 30 ml-bottle (NDC 68462-385-37), b) 60 ml-bottle (NDC 68462-385-02), Rx only, Manufactured by: Glenmark Pharmaceuticals Limited, Baddi Himachal Pradesh 173205, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: Defective Container
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

BUILT BRANDS LLC

Product: Built Bar, Banana Cream Pie Puffs Protein Bar, 1.41 oz. (40…
Reason: Banana Cream Pie Puff Protein Bars have the potential to be contaminated with Escherichia coli.
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAT REAL FOOD LLC

Product: Plant Based Yogurt Culina Mango Orange Blossom Nt Wt 5 oz. (…
Reason: Potential for glass to be found in product
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAT REAL FOOD LLC

Product: Plant Based Yogurt Culina Peach Cashew Nt Wt 5 oz. (142 g) U…
Reason: Potential for glass to be found in product
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAT REAL FOOD LLC

Product: Plant Based Yogurt Culina Strawberry Rose Nt Wt 5 oz. (142 g…
Reason: Potential for glass to be found in product
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAT REAL FOOD LLC

Product: Plant Based Yogurt Culina Plain & Simple Nt Wt 5 oz. (142 g)…
Reason: Potential for glass to be found in product
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAT REAL FOOD LLC

Product: Plant Based Yogurt Culina Bourbon Vanilla Nt Wt 5 oz. (142 g…
Reason: Potential for glass to be found in product
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EAT REAL FOOD LLC

Product: Plant Based Yogurt Culina Blueberry Lavender Nt Wt 5 oz. (14…
Reason: Potential for glass to be found in product
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Prairie City Bakery

Product: Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey…
Reason: Salmonella. Product contains recalled Jif peanut butter as ingredient.
Published: July 13, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass bottle, Rx only, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC 50383-700-16

by Akorn, Inc.

Reason: Defective container: defect prevents product from dispensing as intended.
Published: July 6, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only, 60 mL (2 fl. oz.) bottle, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, N.Y. 11701. NDC: 50383-732-02

by Akorn, Inc.

Reason: Defective Delivery System: Potential defect that could prevent the product from dispensing as intended.
Published: July 6, 2022
Distribution: Nationwide

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Data last updated: September 13, 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.