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Recall totals

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

37,448

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/snack-right-super-foods-inc-dba-brads-raw-chips-recalls-brads-crunchy-kale-veggie-chips-duePublished November 2, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated November 5, 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 OngoingHistorical recordClass II

Daytrana (methylphenidate transdermal system), Delivers 15 mg over 9 hours (1.6 mg/hr), 30 Patches (NDC 68968-5553-1) per box (NDC 68968-5553-3), Rx only, Manufactured for Noven Therapeutics, LLC., Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186.

by Noven Pharmaceuticals Inc

Reason: Defective Delivery System: The number of customer complaints for ripping patches and tight release/adhesive transfer have exceeded the action limits.
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Daytrana (methylphenidate transdermal system), Delivers 10 mg over 9 hours (1.1 mg/hr), 30 Patches (NDC 68968-5552-1) per box (NDC 68968-5552-3), Rx only, Manufactured for Noven Therapeutics, LLC., Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186.

by Noven Pharmaceuticals Inc

Reason: Defective Delivery System: The number of customer complaints for ripping patches and tight release/adhesive transfer have exceeded the action limits.
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 16, 2023Historical recordClass III

Atorvastatin Calcium Tablets, USP 10 mg*, Rx Only, 500 count bottle, Mfd By: Dr. Reddy's Laboratories Limited, Bachupally 500 090, India, NDC 55111-121-05.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities -Degradation Specifications:due to presence of ATV cyclo IP and FP impurities
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 13, 2024Historical recordClass I

NP Thyroid 120 Thyroid Tablets, USP 2 grain (120 mg), packaged in a) 100-count bottles (NDC 42192-328-01) and b) 7-count bottles (NDC 42192-328-07) Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 30005

by Acella Pharmaceuticals, LLC

Reason: Subpotent Drug
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 13, 2024Historical recordClass I

NP Thyroid 60 Thyroid Tablets, USP 1 grain (60 mg) 100-count bottles, Rx Only Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 30005, NDC 42192-330-01

by Acella Pharmaceuticals, LLC

Reason: Subpotent Drug
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 13, 2024Historical recordClass I

NP Thyroid 30 Thyroid Tablets, USP 1/2 grain (30 mg), packaged in a) 100-count bottles (NDC 42192-329-01) and b) 7-count bottles (NDC 42192-329-07), Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 30005

by Acella Pharmaceuticals, LLC

Reason: Subpotent Drug
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 17, 2023Historical recordClass III

Olmesartan Medoxomil Tablets, USP, 20 mg, Rx Only, 30 Tablets, Manufactured by Alkem Laboratories Ltd, Mumbai, 400 013. INDIA, Distributed by: Ascend Laboratories LLC, Parsippany, NJ, 07054, NDC 67877-446-30.

by Ascend Laboratories LLC

Reason: Presence of Foreign Tablet/Capsule
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 24, 2023Historical recordClass I

SARA LEE FROZEN FOODS

Product: Sara Lee Pecan Pie 4oz. retail packaged UPC 032100051118, 24…
Reason: Potentially undeclared peanut
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 11, 2022Historical recordClass II

Brill Inc

Product: 10239710: 12" BAKED CHOCOLATE CHIP MESSAGE COOKIE 14 / 22 oz…
Reason: Potential to contain small foreign objects
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 11, 2022Historical recordClass II

Brill Inc

Product: 10233579 JUMBO CHOCOLATE CHIP COOKIE 12 / 12 INCH BAKED CHOC…
Reason: Potential to contain small foreign objects
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 11, 2022Historical recordClass II

Brill Inc

Product: 10194739 TranSmart" 12 INCH CHOCOLATE CHIP MESSAGE COOKIE 24…
Reason: Potential to contain small foreign objects
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 8, 2021Historical recordClass II

BREW DR KOMBUCHA LLC

Product: Brew Dr. Uplift Mango Passionfruit, Yerba Mate *Guayusa * Gr…
Reason: Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 8, 2021Historical recordClass II

BREW DR KOMBUCHA LLC

Product: Brew Dr. Uplift Blood Orange Lemon, Yerba Mate *Guayusa * Gr…
Reason: Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 8, 2021Historical recordClass II

BREW DR KOMBUCHA LLC

Product: Brew Dr. Uplift Blueberry Raspberry Yerba Mate Guayusa, Gre…
Reason: Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
Published: June 2, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 17, 2022Historical recordClass III

Cequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL each)), Rx only, Manufactured for Sun Pharma Global FZE by: Laboratoire Unither, Coutances, France Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 NDC 47335-506-96

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Subpotent and Presence of Particulates .
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 22, 2022Historical recordClass II

Cefixime for Oral Suspension USP 100 mg/5mL, 50mL HDPE bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc. Baltimore, Maryland, 21202 United States, Manufactured by: Lupin Limited, Manddeep, 462 046, India, NDC 68180-405-01

by Lupin Pharmaceuticals Inc.

Reason: Subpotent Drug
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 5, 2022Historical recordClass II

Delflex Peritoneal Dialysis Solution with 1.5% Dextrose, LM/LC, packaged in a case containing 2 x 6 Liter bags, Rx only, NDC 49230-206-60, Fresenius Medical Care North America, Waltham, MA 02451

by Fresenius Medical Care, North America

Reason: Labeling; Label Mix-up; 4.25% DEXTROSE bag was found inside a 1.5% DEXTROSE box.
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 16, 2021Historical recordClass II

Thumbs Up 7 Blue 69K, 10 capsules, Distributed by Ummzy LLC., Made in USA, UPC 617135894673. Packaged in blister foil sheets in a box. Each box contains 10 capsules.

by Bit & Bet LLC

Reason: Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of sildenafil and tadalafil.
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 28, 2023Historical recordClass III

Dry Eye Test, Fluorescein Sodium, Ophthalmic Strips USP (0.12mg Fluorescein Sodium), 100 Sterile Strips (50 Pouches of 2 Strips Each), Manufactured by: Nomax, Inc, St. Louis, MO 63123, NDC: 51801-008-15

by Nomax Inc

Reason: Subpotent Drug
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 5, 2022Historical recordClass III

Hydrocodone Bitartrate and Homatropine Methlybromide tablets, USP, 5 mg/ 1.5 mg, 30-count bottle, Rx only, Mfd. By:KVK-Tech, Inc., Newtown, PA, 18940 NDC 10702-055-03

by KVK-Tech, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: May 26, 2021
Distribution: Nationwide

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Data last updated: November 5, 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.