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Recall totals

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

37,115

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

State: IN ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 17, 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 I

Morphine Sulfate extended-Release Tablets, USP; 60 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories Inc., NJ; Relabeled by: Bryant Ranch Prepack, Inc, CA, NDC 63629-1089-01

by Bryant Ranch Prepack, Inc.

Reason: Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30 mg Extended-Release tablets may contain Morphine Sulfate 60 mg Extended-Release tablets.
Published: July 20, 2022
Distribution: Distributed to one wholesaler in AL for…

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FDA Recall Terminated Historical recordClass I

Morphine Sulfate extended-Release Tablets, USP; 30 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories Inc., New Brunswick NJ 08901 USA; Relabeled by: Bryant Ranch Prepack, Inc., Burbank, CA, 91504 USA, NDC: 63629-1088-01.

by Bryant Ranch Prepack, Inc.

Reason: Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30 mg Extended-Release tablets may contain Morphine Sulfate 60 mg Extended-Release tablets.
Published: July 20, 2022
Distribution: Distributed to one wholesaler in AL for…

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FDA Recall United States Terminated Historical recordClass I

ARBORYPHARM FOODS INC.

Product: Natreve Vegan Protein Powder 10 servings, 13.1oz (371g), UPC…
Reason: Undeclared allergen; milk.
Published: July 20, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Bakery Barn, LLC

Product: 1st Phorm High Quality Protein Level-1 Bar Chocolate Crunch…
Reason: Protein bar may be contaminated with plastic and paper foreign material
Published: July 20, 2022
Distribution: Distributed to 1 consignee in MO and the…

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FDA Recall United States Terminated Historical recordClass II

Premier Research Labs LLC

Product: AloePro Dietary Supplement Made With Organic ALOE VERA LIQUI…
Reason: Product spoiling over time; spoilage visible beneath lid/closure upon opening.
Published: July 20, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Market Day Local Inc.

Product: Market Day Krabbycakes, Item 3320, Net Wt. 40 oz. (2.5 lbs.)…
Reason: Undeclared shrimp and carmine color
Published: July 20, 2022
Distribution: CA, GA, IL, IN, KS, KY, MD, MI, MO, NC,…

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FDA Recall United States Terminated Historical recordClass I

J & M Foods, Inc.

Product: Favorite Day Lavender Shortbread Cookie Bites Net Wt 7oz (1…
Reason: Undeclared egg and soy lecithin
Published: July 20, 2022
Distribution: Multiple states

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FDA Recall Terminated Historical recordClass II

Estriol 1mg/gm, Vaginal Cream, 30 gm tube, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Drive, 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

Boric Acid 600 mg per suppository, 14 Vaginal Suppositories per box, Wedgewood Village Pharmacy LLC, 405 Heron Drive, 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

Estriol 1mg/gm, Vaginal Cream, 60 gm tube, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Drive, 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

Boric Acid 600 mg capsules, 14 capsules per box, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Drive, 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

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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Data last updated: September 17, 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.