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.

37,066

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

Most affected stateHawaii 200 recalls mention this state

State: RI ×
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 14, 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

Download CSV

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 Terminated Historical recordClass I

Albertsons Companies LLC

Product: Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12…
Reason: Undeclared allergens; fish and shellfish
Published: August 24, 2022
Distribution: U.S. distribution to the following: AK,…

View recall →

FDA Recall United States Terminated Historical recordClass I

Wilbur's Of Maine Chocolate Confections

Product: Wilbur's of Maine Milk Chocolate Covered Blueberries
Reason: Product contains undeclared almonds.
Published: August 24, 2022
Distribution: Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Kabobs Acquisition Inc.

Product: Kabobs The Hors d'oeuvre Specialist TRUFFLE ARANCINI WITH WI…
Reason: The firm was notified by their rice supplier that the product may contain small pieces of glass.
Published: August 24, 2022
Distribution: Product was shipped to the following sta…

View recall →

FDA Recall United States Ongoing Historical recordClass II

Kabobs Acquisition Inc.

Product: Kabobs The Hors d'oeuvre Specialist TOMATO, BASIL & MASCARPO…
Reason: The firm was notified by their rice supplier that the product may contain small pieces of glass.
Published: August 24, 2022
Distribution: Product was shipped to the following sta…

View recall →

FDA Recall United States Terminated Historical recordClass II

Crown Prince, Inc

Product: Crown Prince Quality Natural Seafood Smoked Baby Clams Hand…
Reason: Detectable levels of Per- and polyfluoroalkyl substances (PFAS).
Published: August 24, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL Citrate in 0.9% Sodium Chloride, 2.5 mg per 250 mL, (10 mcg per mL) IV bags, Rx Only, SterRx, 141 Idaho Avenue, Plattsburgh, NY 12903, NDC 70324-327-02.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

FentaNYL Citrate in 0.9% Sodium Chloride 1 mg per 100 mL (10 mcg per mL) IV bags, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY, 12903, NDC 70324-327-01.

by SterRx, LLC

Reason: Lack of Assurance of Sterility
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Prednisone Tablets USP, 20 mg, 100-count bottle, Rx Only, Manufactured by: Strides Pharma Science Ltd., Bengaluru - 562106, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816, NDC 64380-785-06.

by Strides Pharma Inc.

Reason: Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tablets
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Lamotrigine Tablets, USP 100 mg, 1000-count bottles, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-367-10, UPC 3 42291 36710 4

by AVKARE Inc.

Reason: Labeling: Label Error on Declared Strength
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Difluprednate Ophthalmic Emulsion 0.05%, For Ophthalmic Use Only, Sterile, 5 mL bottles, Manufactured by Cipla Ltd., India, Manufactured for: Cipla USA, Inc., NJ 07059, NDC 69097-341-35.

by CIPLA

Reason: Lack of Assurance of Sterility: Complaints received of defective container closure.
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Alcohol Swabsticks, Antiseptic, 50 4" saturated individual packets per box, Manufactured for: Dynarex Corporation, NY 10962, Made in Mexico, NDC 67777-300-01 (current NDC) NDC# 67777-120-10 (discontinued)

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations: products were stored outside the drug label specifications.
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Sterile Alcohol Prep Pads, Sterile, Latex Free, 100 large pads per box, manufactured for: Dynarex Corporation, NY 10962, NDC 67777-121-16.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations: products were stored outside the drug label specifications.
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Racepinephrine Inhalation Solution, USP 2.25%, Bronchodilator, For Oral Inhalation Only, Sulfite Free, Preservative Free, 30 x 0.5 mL Sterile Unit-of-Use Vials, each in a foil pouch, per carton, Nephron Pharmaceuticals Corporation, NDC 0487-5901-99.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations: products were stored outside the drug label specifications.
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Asthmanefrin Racephinephrine Inhalation Solution Bronchodilator, For temporary relief of mild symptoms of intermittent asthma, Preservative Free, Sterile, For Oral Inhalation Only, 30 vials per box, Nephron Pharmaceuticals Corporation, NDC 0487-2784-01.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations: products were stored outside the drug label specifications.
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dakin's Solution, a) sodium hypochlorite 0.125%, quarter strength, NDC 0436-0672-16, b) sodium hypochlorite 0.25%, half strength, NDC 0436-0936-16, c) sodium hypochlorite 0.5% full strength, NDC 0436-0946-16, Antimicrobial, 473 mL (16 fl oz) bottle, Century Pharmaceuticals, Inc.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations: products were stored outside the drug label specifications.
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

A&D Original Ointment, Diaper Rash Ointment & Skin Protectant, 16 oz. Jar, Bayer Healthcare Pharmaceutica, NDC 11523-0096-3.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations: products were stored outside the drug label specifications.
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Pataday, Once Daily Relief, Olopatadine hydrochloride ophthalmic solution 0.2%, Antihistamine, Eye Allergy Itch Relief, Once Daily, Sterile, 2.5 mL (0.085 FL OZ) bottle per box, Alcon, NDC 0065-8150-01.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations: products were stored outside the drug label specifications.
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

GenTeal Tears, Lubricant Eye Ointment, Night-Time Ointment, Sterile, 3.5 gm (0.12 FL OZ) per box, Alcon, NDC 0065-0518-01.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations: products were stored outside the drug label specifications.
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Miralax (Polyethylene Glycol 3350), Powder for Solution, Osmotic Laxative, 30 Once-Daily Doses, Net WT 17.9 OZ (510 g) bottle, Bayer Healthcare Pharmaceuticals, NDC 11523-7234-4.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations: products were stored outside the drug label specifications.
Published: August 17, 2022
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Debrox, Carbamide Peroxide, Earwax Removal Aid, 0.5 FL OZ (15 mL) bottle per box), MedTech Products Inc., NDC 63029-321-01.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations: products were stored outside the drug label specifications.
Published: August 17, 2022
Distribution: Nationwide

View recall →

Data last updated: September 14, 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.