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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 ×
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Recalls announced by month (Year to date)

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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	24,343
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 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 Terminated Historical 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 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 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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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FDA Recall Terminated Historical recordClass II

Sterile Water for Inj., USP, 25 x 100 mL Single Dose Vials per carton, Rx only, For Drug Diluent Use Only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA, NDC Carton: 0409-4887-99; NDC Vial: 0409-4887-25

by Pfizer Inc.

Reason: Presence of Particulate Matter: particulate matter identified as an insect in one vial.
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Triple SupremeZen Plus 3500, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ

by Hyobin LLC

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

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FDA Recall Ongoing Historical recordClass II

PremierZen Black 5000, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ

by Hyobin LLC

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

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FDA Recall Ongoing Historical recordClass II

PremierZen Extreme 3000, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ

by Hyobin LLC

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

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FDA Recall Terminated Historical recordClass III

Asenapine Sublingual Tablets, 10 mg, Rx only, 60 Tablets, Sigmapharm Laboratories, LLC, Bensalem, PA, 19020, NDC 42794-017-10

by SigmaPharm Laboratories LLC

Reason: Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Asenapine Sublingual Tablets, 5 mg, Rx Only, 60 Tablets, Sigmapharm Laboratories, LLC, Bensalem, PA, 19020 NDC 42794-016-10.

by SigmaPharm Laboratories LLC

Reason: Incorrect Product Formulation; product was manufactured with the incorrect Art Cherry Flavor flavoring agent instead of Art Black Cherry Flavor flavoring agent
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Haloperidol Decanoate Injection, USP 100 mg/mL, 1 mL Single Dose Vials, Rx Only, Sterile, 10 Vials, Teva Pharmaceuticals, USA, Inc., North Wales, PA NDC 0703-7131-03

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 2 mL Single-Use Vial, Rx Only, TEVA Parenteral Medicines, Inc. Irvine, CA 92618 NDC 0703-4502-04

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Methylprednisolone Acetate Injectable Suspension USP, 40 mg/mL, 10 mL Multiple Dose Vial, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0703-0045-01

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Haloperidol Decanoate Injection, USP 50 mg/mL, 1 mL Single Dose Vials, Rx Only, Sterile, 10 Vials, Teva Pharmaceuticals, USA, Inc., North Wales, PA NDC 00703-7121-03

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Leucovorin Calcium for Injection, equivalent to leucovorin 350 mg/vial (20 mg/mL), Rx Only, FOR IM or IV Use, Sterile, Teva Parenteral Medicines, Inc., Irvine, CA NDC 0703-5145-01; ALSO LABELED UNDER: NOVAPLUS, Manufactured By: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0703-5145-91 (Novaplus, a registered trademark of Vizient, Inc.)

by Teva Pharmaceuticals USA

Reason: Lack of Assurance of Sterility
Published: May 26, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

CONAGRA BRANDS

Product: Udi Gluten Free Double Chocolate Muffins, 10oz (284g) retail…
Reason: potential presence of an extraneous material (plastic)
Published: May 26, 2021
Distribution: Nationwide

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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.