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Recall totals

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

37,271

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 18, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall OngoingHistorical recordClass II

Carboxymethylcellulose Sodium Ophthalmic Gel 1%, Carboxymethlycellulose Sodium 1% Eye Lubricant, Lubricant Eye Gel, Soothing Gel, Sterile, 0.5 FL OZ (15mL) per bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-066-15.

by BRS Analytical Services, LLC

Reason: cGMP deviations and lack of assurance of sterility.
Published: May 14, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Artificial Tears Ophthalmic Solution, Dextran 70.01%/Glycerin 0.2%/Hypromellose 0.3% (Eye Lubricants) Lubricant Eye Drops, STERILE, 0.5 FL OZ (15 mL) per dropper bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-043-15.

by BRS Analytical Services, LLC

Reason: cGMP deviations and lack of assurance of sterility.
Published: May 14, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 10mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-514-01.

by FDC Limited

Reason: Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
Published: May 14, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Ropivacaine Hydrochloride Injection, USP, 0.5%, 500 mg per 100 mL (5mg/mL), Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Mehsana, India, , Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807 NDC 70121-1734-1 (bag); NDC 70121-1734-3 (box)

by Amneal Pharmaceuticals, LLC

Reason: Presence of Particulate Matter
Published: May 14, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: May 9, 2025Historical recordClass I

Taylor Farms Illinois Inc.

Product: Trader Joe's Sesame Miso Salad with Salmon, net wt. 10.25oz.…
Reason: undeclared milk
Published: May 14, 2025
Distribution: Trader Joe's stores in AL, IA, IL, IN, K…

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FDA Recall United States TerminatedTerminated: September 9, 2025Historical recordClass I

Optimal Carnivore, LLC

Product: Bone & Joint Restore. 180 capsules in a plastic bottle. Shel…
Reason: Potential for contamination with salmonella.
Published: May 14, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, American Regent, Inc., Shirley, NY 11967. NDC carton: 0517-0735-10 / NDC Vial: 0517-0735-01]

by American Regent, Inc.

Reason: Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
Published: May 7, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, Mfd for: Civica, Inc., Lehi, UT 84043,Mfd by: American Regent, Inc., New Albany, OH 43064. NDC Carton: 72572-470-10/ NDC Vial: 72572-470-01.

by American Regent, Inc.

Reason: Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
Published: May 7, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 90 bottles, Rx Only, Manufactured for Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-452-15

by ACCORD HEALTHCARE, INC.

Reason: Subpotent
Published: May 7, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 1000 bottles, Rx Only, Manufactured for Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-450-17

by ACCORD HEALTHCARE, INC.

Reason: Subpotent
Published: May 7, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg), 1000 bottles, Rx Only, Manufactured for Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-448-17.

by ACCORD HEALTHCARE, INC.

Reason: Subpotent
Published: May 7, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 1000 bottles, Rx Only, Manufactured for Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-447-17

by ACCORD HEALTHCARE, INC.

Reason: Subpotent
Published: May 7, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Dexonto 0.4% (dexamethasone sodium phosphate) solution 20 mg/5 mL (4 mg/mL), Rx Only, 12 - 5 mL Single Dose Units per box, Preservative Free, For Iontophoresis Use Only, Non-Sterile Product, Not for Injection, NUBRATORI RX, 381 Van Ness Ave# 1507, CA 90501, NDC 71300-6564-1 (box), 71300-6564-3 (vial).

by Nubratori, Inc

Reason: Labeling: Incorrect or Missing Lot and/or Expiration date: Individual vials of Dexonto 0.4%, are labeled correctly with the BUD of 12/25/2024, however, the outer box on some of the Dexonto 0.4% are labeled incorrectly with a BUD of 12/25/2025.
Published: May 7, 2025
Distribution: PA and CA.

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FDA Recall OngoingHistorical recordClass II

Clindamycin Hydrochloride Capsules, USP, 300mg, 30-count bottles, Manufactured by: Glenmark Pharmaceuticals Limited, NDC 68788-8685-03.

by Preferred Pharmaceuticals, Inc.

Reason: cGMP Deviations
Published: May 7, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Tirofiban Hydrochloride Injection 12.5 mg/250 mL (50 mcg/mL), 250 mL single-dose container (bag), Rx only, Manufactured in India for: Eugia U.S. LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520, NDC 55150-430-01

by Eugia US LLC

Reason: Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
Published: May 7, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Tirofiban Hydrochloride Injection 5 mg/100 mL (50 mcg/mL), 100 mL single-dose container (bag), Rx only, Manufactured in India for: Eugia U.S. LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520, NDC 55150-429-01

by Eugia US LLC

Reason: Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
Published: May 7, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: May 2, 2025Historical recordClass II

Giant Eagle, Inc.

Product: Multigrain Sourdough Freshly Backed, and Half Multigrain Sou…
Reason: Firm is recalling product due to the potential of foreign material (glass)
Published: May 7, 2025
Distribution: The recalled product was distributed to…

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FDA Recall United States TerminatedTerminated: March 17, 2026Historical recordClass II

Gordon Desserts DBA Mochidoki

Product: Sundae Shoppe, Cookies and Cream Mochi Ice Cream, 6 count, 7…
Reason: Undeclared Wheat and Soy
Published: May 7, 2025
Distribution: The recalled product was distributed to…

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FDA Recall United States TerminatedTerminated: July 15, 2025Historical recordClass II

Upper Crust Bakery LP

Product: Whole Grain Multigrain , 20 oz, Paper carton (corrugated),…
Reason: Glass fragment found on top of bread.
Published: May 7, 2025
Distribution: The recalled product was distributed to…

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FDA Recall United States TerminatedTerminated: July 15, 2025Historical recordClass II

Upper Crust Bakery LP

Product: Multigrain Sourdough , 18 oz, Paper carton (corrugated), CP…
Reason: Glass fragment found on top of bread.
Published: May 7, 2025
Distribution: The recalled product was distributed to…

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Data last updated: October 18, 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.