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Recall totals

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

37,060

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/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 9, 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 Ongoing Historical recordClass II

Atorvastatin Calcium Tablets USP, 20 mg, Rx Only, a). 90-count(NDC 67877-512-90), b). 500-count (NDC 67877-512-05), c). 1000-count(NDC 67877-512-10),Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054.

by Ascend Laboratories, LLC

Reason: Failed Dissolution Specifications
Published: October 22, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Atorvastatin Calcium Tablets USP, 40 mg, Rx Only, a). 90-count (NDC 67877-513-90), b). 500-count (NDC 67877-513-05), c). 1000-count (NDC 67877-513-10), Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054.

by Ascend Laboratories, LLC

Reason: Failed Dissolution Specifications
Published: October 22, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Atorvastatin Calcium Tablets USP, 10 mg, Rx Only a) 90-count bottle (NDC 67877-511-90), b). 500-count bottle (NDC 67877-511-05), c). 1000-count bottle (NDC 67877-511-10) Manufactured by: Alkem Laboratories, Ltd. India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054.

by Ascend Laboratories, LLC

Reason: Failed Dissolution Specifications
Published: October 22, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Tavaborole Topical solution 5%, 10 mL bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Changodar, Ahmedabad, India, Distributed by: Viona Pharmaceuticals Inc., Cranford, NJ 07016, NDC 72578-102-04.

by VIONA PHARMACEUTICALS INC

Reason: Discoloration
Published: October 22, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC, 719 Kasota Ave Se, Minneapolis, MN 55414-2842 NDC 71139-0012-1

by IntegraDose Compounding Services LLC

Reason: Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
Published: October 22, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

AMY'S KITCHEN INC.

Product: Gluten Free Bean & Rice Burrito. 12 retail units per case. 5…
Reason: Potential contamination with foreign objects.
Published: October 22, 2025
Distribution: Product distributed to the following sta…

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FDA Recall United States Terminated Historical recordClass II

ONE FROZEN, LLC

Product: Good and Gather brand Southwest-Style Burrito Bowl Blend Pr…
Reason: Product may contain undeclared shrimp (crustacean shellfish).
Published: October 22, 2025
Distribution: Nationwide

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FDA Recall United States Completed Historical recordClass II

Pacific Coast Producers

Product: Pears Halves in Pear Juice from Concentrate; NET WT 15 OZ (4…
Reason: Potential contamination with heavy metal (Lead).
Published: October 22, 2025
Distribution: U.S. distribution: AL, AR, AZ, CA, FL, G…

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FDA Recall United States Completed Historical recordClass II

Pacific Coast Producers

Product: Pears SLICED in Organic Pear Juice from Concentrate; NET WT…
Reason: Potential contamination with heavy metal (Lead).
Published: October 22, 2025
Distribution: U.S. distribution: AL, AR, AZ, CA, FL, G…

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FDA Recall United States Completed Historical recordClass II

Pacific Coast Producers

Product: Halved Pears IN PEAR JUICE FROM CONCNETRATE; NET WT 15 OZ (4…
Reason: Potential contamination with heavy metal (Lead).
Published: October 22, 2025
Distribution: U.S. distribution: AL, AR, AZ, CA, FL, G…

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FDA Recall United States Completed Historical recordClass II

Pacific Coast Producers

Product: Fruit Cocktail IN 100% JUICE WITH ADDED INGREDIENTS; NET WT…
Reason: Potential contamination with heavy metal (Lead).
Published: October 22, 2025
Distribution: U.S. distribution: AL, AR, AZ, CA, FL, G…

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FDA Recall United States Completed Historical recordClass II

NOW Foods

Product: NOW Real Food Organic Unsalted Whole Raw Cashews, 10 oz. pou…
Reason: Undeclared pine nut
Published: October 22, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

NAD+ (Nicotinamide adenine dinucleotide) for Injection, a) 100 mg/mL b) 200 mg/mL, 10 mL multi-dose amber vials, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.

by GenoGenix LLC

Reason: Microbial Contamination of Sterile Products: elevated endotoxin levels
Published: October 15, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Retatrutide for Injection, 60mg / 10mL vial, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692

by GenoGenix LLC

Reason: Lack of Assurance of Sterility
Published: October 15, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Tirzepatide, 60mg/10 mL for Injection, 10mL vial lyophilized, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Extension Health and Synergy Wellness 60mg, 10mL vial lyophilized.

by GenoGenix LLC

Reason: Lack of Assurance of Sterility
Published: October 15, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Semaglutide for Injection, a) 20 mg b) 20 mg/mL, 10 mL Multi-Dose Vials, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for Synergy Wellness, 20 mg, 10mL vial lyophilized.

by GenoGenix LLC

Reason: Lack of Assurance of Sterility
Published: October 15, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Sermorelin Lyophilized powder for reconstitution, 10mg, Vial capacity 10 mL Multi-Dose, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.

by GenoGenix LLC

Reason: Lack of Assurance of Sterility
Published: October 15, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Epithalon for Injection, 20mg, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692 manufactured for Extension Health.

by GenoGenix LLC

Reason: Lack of Assurance of Sterility
Published: October 15, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Tesamorelin for Injection, 15mg, 10 mL Multi-Dose Vial, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.

by GenoGenix LLC

Reason: Lack of Assurance of Sterility
Published: October 15, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Thymosin Beta-4 (TB4) for Injection, 15mg, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.

by GenoGenix LLC

Reason: Lack of Assurance of Sterility
Published: October 15, 2025
Distribution: Nationwide

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Data last updated: September 9, 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.