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

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Source: FDA and USDA public dataLast updated September 8, 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 United States Ongoing Historical recordClass II

A New Life Herbs, LLC

Product: Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea…
Reason: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published: December 31, 2025
Distribution: Multiple states

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FDA Recall United States Ongoing Historical recordClass II

A New Life Herbs, LLC

Product: Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to…
Reason: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Published: December 31, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

Silvestri Sweets Inc dba Carousel Candies

Product: Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz.…
Reason: Undeclared pecan
Published: December 31, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Silvestri Sweets Inc dba Carousel Candies

Product: Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pou…
Reason: Undeclared wheat
Published: December 31, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Lil Turtles LLC

Product: Grandma Belle's Tomato Basil Soup, Net Wt. 17 oz. (482g), pa…
Reason: Undeclared allergen - milk
Published: December 31, 2025
Distribution: Multiple states

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FDA Recall Ongoing Historical recordClass II

Ciclopirox Shampoo, 1%, 120 mL, Rx only, Mfg by: Taro Pharmaceuticals Inc., Ontario, Canada; Dist. by: Taro Pharmaceuticals USA, Inc., NY 10532. NDC 51672-1351-08

by SUN PHARMA /TARO

Reason: Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Cisatracurium Besylate Injection USP, 20 mg/10 mL*,(2 mg/mL), 10 x 10 mL Multiple-dose Vials per carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, 10mL Multiple-dose vial, NDC 70069-161-01; 10x10mL Multiple-dose vials per Carton, NDC 70069-161-01.

by SOMERSET THERAPEUTICS LLC

Reason: Subpotent product:out of specification assay results observed during long term stability testing.
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Cisatracurium Besylate Injection USP, 200mg/20mL*(10mg/mL), 10 x 20 mL Single-dose Vials per Carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, Single dose 20mL vial NDC 70069-151-01; 10 x 20 Single dose vials per Carton, NDC 70069-151-10.

by SOMERSET THERAPEUTICS LLC

Reason: Subpotent product:out of specification assay results observed during long term stability testing.
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Cisatracurium Besylate Injection USP, 10 mg/5 mL* (2mg/mL), 10 x 5 mL Single-dose Vials per Carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, Single-dose 5 mL vial NDC 70069-141-01; 10x5 mL single dose vial per Carton NDC 70069-141-10.

by SOMERSET THERAPEUTICS LLC

Reason: Subpotent product:out of specification assay results observed during long term stability testing.
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 93012 USA. NDC 51407-973-10

by Golden State Medical Supply Inc.

Reason: Presence of Foreign Tablets/Capsules
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

OraVerse, (Phentolamine Mesylate) Injection, 0.4 mg/1.7mL, packaged in a carton containing 10 cartridges, 0.4 mg/1.7mL, Rx only, Made in Canada by Novocol Pharmaceutical of Canada, Inc., Distributed by Septodont, Inc., Louisville, Co, 80027, NDC 0362-0101-10

by Novocol Pharmaceutical of Canada, Inc.

Reason: Defective container: cracked/broken cartridges
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Cook-Walte, Carbocaine 3% (30 mg/mL), (mepivacaine hydrochloride Injection, USP), packaged in a carton containing 50 Single-Dose Cartridges, 1.7 mL, Rx only, Manufactured by Novocol Pharmaceutical of Canada, Inc., NDC 0362-0753-05.

by Novocol Pharmaceutical of Canada, Inc.

Reason: Defective container: cracked/broken cartridges
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Benco dental Graham CHEMICAL CO., Mepivacaine HCI 3% (30 mg/mL) Injection, [Mepivacaine HCI Injection, USP], packaged in a carton containing 50 single-dose Cartridges, 1.7 mL each, Rx only, Distributed by Benco Dental 295 Center Point Blvd, Pittston, PA 18640, Manufactured by Novocol Pharmaceutical of Canada, Inc., NDC 66975-406-51.

by Novocol Pharmaceutical of Canada, Inc.

Reason: Defective container: cracked/broken cartridges
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

darby dental supply, MEPIVACAINE, Mepivacaine HCI 3% (30mg/mL) Injection, [Mepivacaine HCI Injection, USP], packaged in a carton containing 50 single-dose Cartridges, 1.7 mL each, Rx only, Manufactured by Novocol Pharmaceutical of Canada, Inc., NDC 66467-9760-5.

by Novocol Pharmaceutical of Canada, Inc.

Reason: Defective container: cracked/broken cartridges
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

3% Polocaine DENTAL, Mepivacaine Hydrochloride 3% (30mg/mL) (Mepivacaine HCI Injection, USP), packaged in a carton containing 50 single-dose Cartridges, 1.7 ml each, Rx only, Manufactured for Dentsply Pharmaceutical, York, PA 17404, by Novocol Pharmaceutical of Canada, Inc., NDC 66312-441-16.

by Novocol Pharmaceutical of Canada, Inc.

Reason: Defective container: cracked/broken cartridges
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lidocaine HCI 2% and Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose Cartridges, 1.7 ml each, Rx only, Manufactured for Patterson Dental Supply, Inc., 1031 Mendota Heights Road, Saint Paul, MN55120, Manufactured by: Novocol Pharmaceutical of Canada, Inc., NDC 50227-1030-5.

by Novocol Pharmaceutical of Canada, Inc.

Reason: Defective container: cracked/broken cartridges
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

2% Xylocaine DENTAL with Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose cartridges, 1.7 mL each, Rx only, Manufactured for Dentsply Pharmaceutical, York, PA 17404, by Novocol Pharmaceutical of Canada, Inc., NDC 66312-176-16.

by Novocol Pharmaceutical of Canada, Inc.

Reason: Defective container: cracked/broken cartridges
Published: December 24, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Lexunder Inc

Product: Food to Live brand ORGANIC SUPERGREENS POWDER MIX, packaged…
Reason: Contaminated with Salmonella
Published: December 24, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

Lexunder Inc

Product: Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged hea…
Reason: Contaminated with Salmonella
Published: December 24, 2025
Distribution: Multiple states

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FDA Recall Ongoing Historical recordClass II

Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-09.

by Lupin Pharmaceuticals Inc.

Reason: Defective container - seal not adhering to bottles
Published: December 17, 2025
Distribution: Nationwide

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Data last updated: September 8, 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.