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

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Source: FDA and USDA public dataLast updated October 19, 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

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

FDA Recall United States OngoingHistorical recordClass II

Chicken of the Sea; Thai Union

Product: Genova branded Solid white Tuna; In Olive Oil; Wild Caught;…
Reason: Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Nelarabine Injection, 250mg/50mL, (5mg/mL), packaged in: a) 50 mL Single-Dose Vial, NDC 70710-1839-1; b) 6 x 50 mL Single-Dose Vial, NDC 70710-1839-8, Rx only, Manufactured by Zydus Lifesciences Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc, Pennington, NJ

by Zydus Pharmaceuticals (USA) Inc

Reason: Failed Impurities/Degradation Specifications
Published: March 12, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Nelarabine Injection, 250mg/50mL, (5mg/mL), packaged in: a) 50 mL Single-Dose Vial, NDC 70710-1726-1; b) 6 x 50 mL Single-Dose Vial, NDC 70710-1726-8, Rx only, Manufactured by Zydus Lifesciences Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc, Pennington, NJ

by Zydus Pharmaceuticals (USA) Inc

Reason: Failed Impurities/Degradation Specifications
Published: March 12, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Morphine Sulfate 5 mg per 0.25 mL Oral Syringe, Delivers: 0.25 mL, Oral Solution, Rx Only, Mfg by: Hikma, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: a) 00406800312, b) 00406800330, c) 00054051750.

by Safecor Health, LLC

Reason: Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
Published: March 12, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Lorazepam 0.5 mg per 0.25 mL Oral Syringe, Delivers: 0.25 mL, Oral Concentrate, Rx Only, Refrigerate, Mfg by: PAI, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: a) 00054353244, b) 00121077001, c) 65162068784.

by Safecor Health, LLC

Reason: Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
Published: March 12, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe, Delivers: 0.5 mL, Iron Supplement Drops, Mfg by: Akron Pharma, Pkg by: Safecor, Columbus, OH 43204. NDC: a) 71399748005, b) 39328055750, c) 69618007059.

by Safecor Health, LLC

Reason: Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
Published: March 12, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Simethicone 20 mg per 0.3 mL Oral Syringe, Delivers: 0.3 mL, Oral Drops, Mfg By: Rugby, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 00536130375.

by Safecor Health, LLC

Reason: Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
Published: March 12, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) per 0.05 mL Oral Syringe, Delivers: 0.05 mL Oral Solution, Mfg by: Westminster, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 69367028302.

by Safecor Health, LLC

Reason: Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
Published: March 12, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Morphine Sulfate Extended-Release Tablets, 100 mg, 100-count bottles, Rx Only, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901. Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512. NDC 63304-452-01

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Dissolution Specifications
Published: March 12, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 8, 2025Historical recordClass I

Amazon Retail LLC

Product: ASIN B0CY2RDW5T, Amazon Fresh brand, Bake at Home Jumbo Suga…
Reason: Undeclared egg.
Published: March 12, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 8, 2025Historical recordClass I

Amazon Retail LLC

Product: ASIN B084PZ7K98, Amazon Fresh Jumbo Sugar Cookie, 27 oz (12…
Reason: Undeclared egg.
Published: March 12, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 21, 2026Historical recordClass I

JFE FRANCHISING INC

Product: Chef Salad 11 oz packed in clamshells
Reason: Potential to be contaminated with Salmonella
Published: March 12, 2025
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: September 21, 2026Historical recordClass I

JFE FRANCHISING INC

Product: Family Cobb Salad 22 oz Cobb Salad 11 oz packed in clamshel…
Reason: Potential to be contaminated with Salmonella
Published: March 12, 2025
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: September 21, 2026Historical recordClass I

JFE FRANCHISING INC

Product: Mixed Melon, Cucumber & Tajin 18 oz Watermelon & Cucumber w/…
Reason: Potential to be contaminated with Salmonella
Published: March 12, 2025
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: September 21, 2026Historical recordClass I

JFE FRANCHISING INC

Product: Vegetable Bowl 13 oz Small Vegetable Tray 19.5 oz Vegetable…
Reason: Potential to be contaminated with Salmonella
Published: March 12, 2025
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: September 21, 2026Historical recordClass I

JFE FRANCHISING INC

Product: Cucumber, Lime & Tajin 19 oz Cucumber with Ranch 9 oz Cucumb…
Reason: Potential to be contaminated with Salmonella
Published: March 12, 2025
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: September 21, 2026Historical recordClass I

JFE FRANCHISING INC

Product: Garden Salad 12 oz Family Garden Salad 24 oz packed in clam…
Reason: Potential to be contaminated with Salmonella
Published: March 12, 2025
Distribution: Multiple states

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FDA Recall CompletedTerminated: February 26, 2026Historical recordClass II

Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection Only, Office Use Only - Not for Resale - Single Use, This drug product was repackaged by Turbare Manufacturing, 925 Jeanette Drive, Conway, AR 72032, NDC: 83556-0101-01.

by Turbare Manufacturing

Reason: Lack of Assurance of Sterility: due to a quality control process deviation
Published: March 5, 2025
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

Estradiol Gel, 0.1%, 0.25 mg/g, 30 packets per carton, Rx Only, For Topical Use Only, Manufactured by Padagis, Yeruham, Israel, NDC: 45802-0134-30

by Padagis US LLC

Reason: Defective Container: Some packets may not be fully sealed, potentially allowing for loss of Ethanol from the product.
Published: March 5, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 21, 2025Historical recordClass II

V Chocolates, Inc

Product: Assorted Chocolate Caramels with kosher sea salt, Net Weight…
Reason: Small pieces of plastic broken tray in the product.
Published: March 5, 2025
Distribution: Nationwide

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Data last updated: October 19, 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.