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Recall totals

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

37,118

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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 20, 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

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass III

Laboratorios Pisa Sa De Cv

Product: Electrolit Fruit Punch Zero, 625ML/21OZ packaged in a polypr…
Reason: Product contains undeclared FD&C Red No. 40.
Published: March 24, 2021
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass III

Laboratorios Pisa Sa De Cv

Product: Electrolit Ponche/Fruit Punch; in 625 mL/21 oz and 300ML/10o…
Reason: Product contains undeclared FD&C Red No. 40.
Published: March 24, 2021
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

Seafood Imports Distributors Inc.

Product: Java Frozen Tuna Steaks - 10 oz. Net Wt. 10 lb. - Approxima…
Reason: FDA Sample found Salmonella in one lot of 10 oz. frozen tuna steaks.
Published: March 24, 2021
Distribution: Multiple states

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FDA Recall Terminated Historical recordClass III

Menopur 75 IU, (menotropins for injection), packaged as a) 5 single dose vials of Menotropins for injection, 5 single dose vials of 0.9% Sodium Chloride Injection, USP 2 mL, NDC 55566-7501-2; b) Professional Sample Kit: 3 single dose vials of Menotropins for injection, 3 single dose vials of 0.9% Sodium Chloride Injection, USP 2 mL, NDC 55566-7501-3; Rx Only, Manufactured for Ferring Pharmaceuticals Inc. Parsippany. NJ 07054. Diluent manufactured for Ferring Pharmaceuticals Inc.

by Ferring Pharmaceuticals Inc

Reason: Failed pH specifications: Out of Specification pH results for 0.9% Sodium Chloride, USP
Published: March 17, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

GREEN CITY DISTRIBUTION

Product: Al-Riyan Tuna Meat in Vegetable oil 7 oz. can 48 cans per…
Reason: High levels of histamines
Published: March 17, 2021
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Westminster Cracker Inc.

Product: Old Cape Cod Soup and Chowder Oyster Crackers - 8oz Box, 12…
Reason: Product may contain hard plastic foreign object.
Published: March 17, 2021
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass III

One Degree Organic Foods Inc,

Product: One Degree Organic Foods Gluten Free Sprouted Rolled Oats NE…
Reason: Rancidity and packaging integrity defects in GF sprouted rolled oats
Published: March 17, 2021
Distribution: Distributed to Costco retail locations i…

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FDA Recall Terminated Historical recordClass III

Methylprednisolone Tablets USP, 4 MG, packaged in a 21-count blister pack, Rx only, Jubilant Cadista Pharmaceuticals, Inc., Salisbury, MD 21801, NDC 59746-001-03

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Labeling: Illegible label: Customer complaint received of mis-alignment print of the printed dosing instructions on the blister card.
Published: March 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 25x2mL Single Dose Vials, Rx only, Distributed by Teva Pharmaceuticals, USA, Inc., Parsippany, NJ Vial NDC 0703-4502-01 (vial) NDC# 0703-4502-04 (tray)

by Teva Pharmaceuticals USA

Reason: Chemical contamination; Unknown brown residue adhering to the inside of one vial.
Published: March 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours (3.3 mg/hr) Contains: 30 Patches in a foil-sealed polypropylene tray, packed in a paper carton, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL, 33186, By Noven Pharmaceuticals, Inc., Miami, FL, 33186, NDC 68968-5555-3.

by Noven Pharmaceuticals Inc

Reason: Defective Delivery System: Out of specification for mechanical peel.
Published: March 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours (2.2 mg/hr) Contains: 30 Patches in a foil-sealed polypropylene tray, packed in a paper carton, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL, 33186, By Noven Pharmaceuticals, Inc., Miami, FL, 33186, NDC 68968-5554-3.

by Noven Pharmaceuticals Inc

Reason: Defective Delivery System: Out of specification for mechanical peel.
Published: March 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system), Delivers 15 mg over 9 hours (1.6 mg/hr), Contains: 30 Patches in in a foil-sealed polypropylene tray, packed in a paper carton, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL, 33186, By Noven Pharmaceuticals, Inc., Miami, FL, 33186, NDC 68968-5553-3.

by Noven Pharmaceuticals Inc

Reason: Defective Delivery System: Out of specification for mechanical peel.
Published: March 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system), Delivers 10 mg over 9 hours (1.1 mg/hr), Contains: 30 Patches in a foil-sealed polypropylene tray, packed in a paper carton, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL, 33186, By Noven Pharmaceuticals, Inc., Miami, FL, 33186, NDC 68968-5552-3.

by Noven Pharmaceuticals Inc

Reason: Defective Delivery System: Out of specification for mechanical peel.
Published: March 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Progesterone Capsules, 200 mg, 100-count bottles, Rx Only, MADE IN FRANCE; Distributed by: Dr. Reddy's Laboratories, Inc., Princeton, NJ 08540; NDC 43598-350-01.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Dissolution Specifications: Out-of-specification results observed for dissolution during stability testing.
Published: March 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Atorvastatin Calcium Tablets, 40mg, packaged in a) 90-count bottles, NDC 55111-123-90; b) 500-count bottles, NDC 55111-123-05; Rx only, Mfd By: Dr. Reddy's Laboratories Limited Srikakulam - 532 409 INDIA

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradation Specifications:presence of ATV cyclo IP and FP, Dihydroxy epoxy and Dieto epoxy impurities
Published: March 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Famotidine Tablets USP 40mg, 1,000-count bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 Made in India, NDC 65862-860-99

by Aurobindo Pharma USA Inc.

Reason: Presence of foreign tablets/capsules: Famotidine 20mg and ibuprofen 400mg tablets were found in a lot of famotidine 40mg.
Published: March 10, 2021
Distribution: Multiple states

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FDA Recall Terminated Historical 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 NDC 47335-506-96

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Subpotent
Published: March 10, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Ferrara Candy Company

Product: Ferrara Candy Company assorted candy Heart Box, including La…
Reason: Undeclared ingredients on retail packaging, including but not limited to certified colors Red #40 and Blue #1
Published: March 10, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Urban Remedy

Product: Urban Remedy Organic Almond Maca Almond Milk; 16 FL. OZ (47…
Reason: Firm discovered that labeling had been switched for two products on one day of production - undeclared almonds and cashews.
Published: March 10, 2021
Distribution: CA only

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FDA Recall United States Terminated Historical recordClass II

Urban Remedy

Product: Urban Remedy Organic Cacao Mocha Cold Brew Coffee; 16 FL. O…
Reason: Firm discovered that labeling had been switched for two products on one day of production - undeclared almonds and cashews.
Published: March 10, 2021
Distribution: CA only

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Data last updated: September 20, 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.