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Recall totals

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

37,061

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 recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 10, 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

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Terminated Historical recordClass III

Tolterodine Tartrate Extended-Release Capsules, 2 mg, 30 Capsules (3 x 10) Unit Dose carton, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA, NDC 0904-6592-04.

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason: Failed Dissolution Specifications: Out of specification results obtained during routine stability testing for dissolution.
Published: April 9, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

FRUSELVA USA

Product: Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Pur…
Reason: elevated level of lead
Published: April 9, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Seabear Company

Product: SeaBear Smokedhouse Alehouse Clam Chowder is packaged in ret…
Reason: Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
Published: April 9, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Seabear Company

Product: SeaBear Smokedhouse Salmon Chowder is packaged in flexible r…
Reason: Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
Published: April 9, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

8.4% Sodium Bicarbonate Injection, USP, 50 mEq/50 mL (1 mEq/mL), 25 x 50 mL Single Dose Vials per carton, For Intravenous Use Only, Rx Only, Manufactured by: Exela Pharma Sciences, LLC, Lenoir, NC 28645. NDC Inner Vial: 51754-5001-1; NDC Carton: 51754-5001-4

by Exela Pharma Sciences LLC

Reason: Lack of Assurance of Sterility
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

SinuCleanse Soft Tip NETI POT Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 kettle style Neti Pot, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00102 7

by Ascent Consumer Products Inc.

Reason: Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

SinuCleanse Premixed SALINE PACKETS (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg) for Nasal Wash System, 60-count All Natural USP Grade Saline Packets, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00103 4

by Ascent Consumer Products Inc.

Reason: Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 Soft tip Squeeze Bottle, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00104 1

by Ascent Consumer Products Inc.

Reason: Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

babyganics, Sheer Blend, SPF 50 Mineral Sunscreen Fragrance Free (zinc oxide 20%), a) 1.7 FL OZ (50 mL) bottle, UPC 810035921658, b) 8 FL OZ (236 mL) bottle, UPC 810035921382, Dist. by KAS Direct, LLC, 1525 Howe St., Racine, WI 53403, Made in Canada.

by Johnson, S C and Son, Inc

Reason: Failed stability specifications: during routine stability monitoring quality concerns were identified. Physical separation for ingredients was observed.
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.2% ROPivacaine HCl 200 mg/100 mL (2 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Use Only, QuVa Pharma, 1075 West Park One Drive, Suite 100, Sugar Land, Tx 77478. NDC: 70092-1259-75

by QuVa Pharma, Inc.

Reason: Lack of Assurance of Sterility
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine HCl 125 mg/100 mL (1.25 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Use Only, QuVa Pharma, 1075 West Park One Drive, Suite 100, Sugar Land, Tx 77478. NDC: 70092-1255-75

by QuVa Pharma, Inc.

Reason: Lack of Assurance of Sterility
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.1% Bupivacaine HCl 100 mg/100 mL (1 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Use Only, QuVa Pharma, 1075 West Park One Drive, Suite 100, Sugar Land, Tx 77478. NDC: 70092-1255-75

by QuVa Pharma, Inc.

Reason: Lack of Assurance of Sterility
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Testosterone Gel 1%, 5 grams, 30 Unit-dose Packets in a carton, Rx only, Distributed by: Strides Pharma Inc., East Brunswick, NJ, NDC 64380-152-02

by Strides Pharma, Inc.

Reason: Presence of foreign substance: Presence of Benzene.
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Testosterone Gel 1%, 2.5 grams, 30 Unit-dose packets in a carton, Rx only, Distributed by: Strides Pharma Inc., East Brunswick, NJ, NDC 64380-151-02

by Strides Pharma, Inc.

Reason: Presence of foreign substance: Presence of Benzene.
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

METFORMIN HYDROCHLORIDE EXTENDED- RELEASE 500MG, 180 TABLETS, Packaged BY: A-S Medication Solutions, Libertyville, IL 60048 NDC 50090-1494-3.

by A-S Medication Solutions LLC

Reason: Presence of Foreign Tablets/Capsules.
Published: April 2, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Massimo Zanetti Beverage USA

Product: COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY…
Reason: Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.
Published: April 2, 2025
Distribution: Product was shipped to distribution cent…

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in India, NDC 51079-443-20.

by Mylan Institutional, Inc.

Reason: Super-Potent Drug: Out of specification potency results were obtained.
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in India, NDC 51079-445-20.

by Mylan Institutional, Inc.

Reason: Super-Potent Drug: Out of specification potency results were obtained.
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

CURAD Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per Carton, 30 Boxes per Case, Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093, USA, Made in India, www.curad.com, 1-800-633-5463, NDC 53329-827-30.

by MEDLINE INDUSTRIES, LP - Northfield

Reason: Subpotent Drug
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Medline Alcohol Prep Pads, 70% Isopropyl Alcohol, 100 Sterile 2-Ply Pads, Single Use Only, Large, www.medline.com, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093 USA, 1-800-MEDLINE, NDC 53329-811-30.

by MEDLINE INDUSTRIES, LP - Northfield

Reason: Subpotent Drug
Published: March 26, 2025
Distribution: Nationwide

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Data last updated: September 10, 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.