Data Explorer

Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,113

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

State: AS ×
Clear all

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

Filters

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated September 15, 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

Download CSV

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 II

Vumerity (diroximel fumarate) delayed-release capsule, 231 mg, packaged in a) 106-count bottle, b)120-count bottle, Rx only, Manufactured for: Biogen Inc., Cambridge, MA 02142, NDC 64406-020-01

by Biogen MA Inc.

Reason: Failed dissolution specifications: out-of-specification test results observed during the buffer stage dissolution testing.
Published: December 23, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lansoprazole Delayed-Release Orally Disintegrating Tablets, 30 mg, 100 Tablets (10 x 10 unit-dose) blister pack, Rx only, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534 NDC 68382-772-77

by Zydus Pharmaceuticals (USA) Inc

Reason: Failed Dissolution Specifications
Published: December 23, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg, 100 Tablets (10x10 unit dose) blister pack, Rx only, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534 NDC 68382-771-77

by Zydus Pharmaceuticals (USA) Inc

Reason: Failed Dissolution Specifications
Published: December 23, 2020
Distribution: Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Fusion Health and Vitality LLC

Product: PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY…
Reason: The firm is recalling their products due the unapproved use of a food additive and unapproved marketing statements
Published: December 23, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Scandonest 3% Plain (Mepivacaine Hydrochloride 3% without Vasoconstrictor), packaged in cartons of 50 cartridges (1.7 mL each), Rx only, Manufactured for SEPTODONT, Inc., Louisville, CO 80027, by Novocol Pharmaceutical of Canada, Inc., Cambridge, ON N1R 6X3, Canada, NDC 0362-1098-90

by Novocol Pharmaceutical of Canada, Inc.

Reason: Labeling: Label mix-up
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Docetaxel Injection USP 160 mg/8mL (20 mg/mL), For Intravenous Infusion Only, Rx Only, 8 mL Single Use Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, NDC 72485-216-08.

by Shilpa Medicare Limited

Reason: CGMP Deviations
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Imatinib Mesylate Tablets 400 mg, Rx Only, 30-count Bottle, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals Inc., Manalapan, NJ 07726, NDC 72485-203-30.

by Shilpa Medicare Limited

Reason: CGMP Deviations
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Imatinib Mesylate Tablets 100 mg, Rx Only, 90-count Bottle, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals Inc., Manalapan, NJ 07726, NDC 72485-202-90.

by Shilpa Medicare Limited

Reason: CGMP Deviations
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Azacitidine for Injection 100 mg/vial, For Subcutaneous and Intravenous Use Only, Rx Only, One Single Dose Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, NDC 72606-558-01.

by Shilpa Medicare Limited

Reason: CGMP Deviations
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Azacitidine for Injection 100 mg/vial, For Subcutaneous and Intravenous Use Only, Rx Only, One Single Dose Vial, Cytotoxic Agent, Manufactured by: Shilpa Medicare Limited, Jadcherla, 509301, India, Distributed by: Armas Pharmaceuticals, Inc. Manalapan, NJ 07726 NDC 72485-201-01.

by Shilpa Medicare Limited

Reason: CGMP Deviations
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Busulfan Injection 60 mg/10 mL (6 mg/mL), For Intravenous Infusion Only, Must be diluted before use, Single Dose Vial, Sterile, Cytotoxic Agent, Rx Only, 10 mL vial, Manufactured by: Shilpa Medicare Limited, India, Distributed by: Armas Pharmaceuticals, Inc., Manalapan, NJ 07726, Vial NDC 72485-210-01, Carton NDC 72485-210-08.

by Shilpa Medicare Limited

Reason: CGMP Deviations
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL Single Dose Bottle, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-671-05

by Fresenius Kabi USA, LLC

Reason: Cross Contamination with other products: trace amounts of lidocaine
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

JMH International, LLC

Product: Chef Myron's Premium Shoyu Sauce, 1 GAL (3.78 L), Item # 400…
Reason: Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

JMH International, LLC

Product: Chef Myron's Yakitori Sauce, 64 FL OZ (1.89 L), Item # 4000…
Reason: Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

JMH International, LLC

Product: Chef Myron's Tsukeyaki Sauce, 64 FL OZ (1.89 L), Item # 4000…
Reason: Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

JMH International, LLC

Product: Chef Myron's Tangy Teriyaki Sauce, 64 FL OZ (1.89 L), Item #…
Reason: Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

JMH International, LLC

Product: Chef Myron's Szechuan Sauce, 64 FL OZ (1.89 L), Item # 40002…
Reason: Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

JMH International, LLC

Product: Chef Myron's Premium Teriyaki Sauce, 64 FL OZ (1.89 L), Item…
Reason: Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

JMH International, LLC

Product: Chef Myron's Ponzu Sauce, 64 FL OZ (1.89 L), Item # 40002311…
Reason: Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.
Published: December 16, 2020
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

JMH International, LLC

Product: Chef Myron's Eurasian Fusion Sauce, 64 FL OZ (1.89 L), Item…
Reason: Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.
Published: December 16, 2020
Distribution: Nationwide

View recall →

Data last updated: September 15, 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.