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Recall totals

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

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated November 8, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

Sore Throat & Laryngitis Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7014-7

by Beaumont Bio-med, Inc.

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: September 26, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

Sinus Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7013-7

by Beaumont Bio-med, Inc.

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: September 26, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 16, 2022Historical recordClass II

Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7002-7

by Beaumont Bio-med, Inc.

Reason: CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published: September 26, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 1, 2022Historical recordClass II

Tizanidine HCl Tablets, USP 2mg, 150-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited Srilakulam - 532 409 INDIA, NDC 55111-179-15, UPC 35511179153

by Dr. Reddy's Laboratories, Inc.

Reason: Presence of Foreign Tablets/Capsules: Glimepiride tablet was found in a bottle of Tinzadine Hcl Tablets .
Published: September 26, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 1, 2020Historical recordClass II

0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Healthcare Corporation Deerfield, IL 60015 -- NDC 0338-0049-31

by Baxter Healthcare Corporation

Reason: cGMP Deviation
Published: September 26, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 2, 2019Historical recordClass I

Norepinephrine 4 mg (16 mcg/mL) added to 5% Dextrose 250 mL Bag Preservative Free, Rx only, QuVa Pharma, 519 Route 173, Bloombury, NJ 08804, UPC 70092103417.

by QuVa Pharma, Inc.

Reason: Subpotent Drug: Product may not have the active ingredient present in the bag.
Published: September 26, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 7, 2020Historical recordClass I

Hydrochlorothiazide Tablets USP, 12.5 mg, 100-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703; Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad - 382 210, India; NDC 16729-182-01.

by ACCORD HEALTHCARE, INC.

Reason: Product Mix-Up: customer complaint that a sealed bottle labeled as Hydrochlorothiazide Tablets USP 12.5 mg contained only Spironolactone Tablets USP 25 mg.
Published: September 19, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 27, 2021Historical recordClass I

Respitrol, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-003-02

by Hellolife

Reason: Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia
Published: September 19, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 27, 2021Historical recordClass I

Thyroveev, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-025-02

by Hellolife

Reason: Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia
Published: September 19, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 27, 2021Historical recordClass I

Neuroveen, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-015-02

by Hellolife

Reason: Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia
Published: September 19, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 27, 2021Historical recordClass I

Compulsin, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-034-02

by Hellolife

Reason: Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia
Published: September 19, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 14, 2019Historical recordClass III

Diltiazem HCl Extended-Release Capsules, USP 120 mg 500-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505. NDC 0378-5220-05

by Mylan Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stability testing for related compound.
Published: September 19, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 14, 2019Historical recordClass III

Diltiazem HCl Extended-Release Capsules, USP 120 mg 100-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505. NDC 0378-5220-01

by Mylan Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications: Out of specification test results obtained during routine stability testing for related compound.
Published: September 19, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 6, 2019Historical recordClass III

Pramipexole dihydrochloride extended release tablets, 0.75 mg, packaged in 30-count bottles, Rx only, Manufactured by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 10370-252-11

by Par Pharmaceutical, Inc.

Reason: Failed impurities/degradation specifications: Finished product contain a known product impurity about current specification levels.
Published: September 19, 2018
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 26, 2020Historical recordClass III

Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 2.5 mL Single-use Vial, Rx only, Sterile, Manufactured for: Hospira, Inc, Lake Forest, IL 60045 USA. NDC: 0409-1140-01

by Pfizer Inc.

Reason: Failed Impurities/Degradation Specifications; Out of specification stability testing results at the 18 month time point
Published: September 19, 2018
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: July 19, 2019Historical recordClass II

Air Stream Corp.

Product: Shredded green cabbage
Reason: The product may be contaminated with Listeria monocytogenes.
Published: September 19, 2018
Distribution: Massachusetts, New York, New Jersey, Con…

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FDA Recall United States TerminatedTerminated: July 19, 2019Historical recordClass II

Air Stream Corp.

Product: Radicchio, 10 lbs
Reason: The product may be contaminated with Listeria monocytogenes.
Published: September 19, 2018
Distribution: Massachusetts, New York, New Jersey, Con…

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FDA Recall United States TerminatedTerminated: July 19, 2019Historical recordClass II

Air Stream Corp.

Product: Brussel Sprouts
Reason: The product may be contaminated with Listeria monocytogenes.
Published: September 19, 2018
Distribution: Massachusetts, New York, New Jersey, Con…

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FDA Recall United States TerminatedTerminated: July 19, 2019Historical recordClass II

Air Stream Corp.

Product: Green Kale
Reason: The product may be contaminated with Listeria monocytogenes.
Published: September 19, 2018
Distribution: Massachusetts, New York, New Jersey, Con…

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FDA Recall United States TerminatedTerminated: July 19, 2019Historical recordClass I

Air Stream Corp.

Product: Salad Mix (Endive, Chicory, Romaine, Escarole, and Radicchio…
Reason: The product may be contaminated with Listeria monocytogenes.
Published: September 19, 2018
Distribution: Massachusetts, New York, New Jersey, Con…

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Data last updated: November 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.