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Recall totals

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

36,949

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,732

Class I recallsReasonable probability of serious health consequences

24,263

Class II recallsTemporary or medically reversible health consequences

2,873

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 2,071 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foods-alive-recalls-organic-moringa-leaf-powder-because-possible-health-riskPublished September 4, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 6, 2026 ET

Summary (Year to date)

1,458 recalls have been announced year to date.
Aug 2026 was 53% 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	24,263
Class I	9,732
Class III	2,873
Not Yet Classified	1

Recalls by class
Class	Recalls
Class II	24,263
Class I	9,732
Class III	2,873
Not Yet Classified	1

FDA Recall Ongoing 2026 recordClass II

exchange select, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Menthol Flavor, 30-count bag, Manufactured for Your Military Exchanges By: Medical Group Care, LLC, 1035 Collier Center Way, STE 5, Naples, FL, Made in China, NDC: 83698-581-30, UPC: 614299398887.

by Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

Reason: This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
Published: April 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

exchange select, Menthol -Cough Suppressant Oral Anesthetic, Honey Lemon Flavor Cough Drops, 30-count bag, Manufactured for Your Military Exchanges By: Medical Group Care, LLC., 1035 Collier Center Way, STE 5, Naples, FL, Made in China, NDC 83698-580-30, UPC: 614299398870.

by Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

Reason: This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
Published: April 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

SLMD Benzoyl Peroxide Acne Lotion, Benzoyl Peroxide 2.5%, a) 0.7 fl. oz - 21 mL and b) 1.5 fl. oz. - 44mL bottles, SANDRA LEE MD., Distributed by Skin PS Brands, Culver City, CA 90232.

by Owen Biosciences Inc.

Reason: Chemical contamination: Presence of benzene
Published: April 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

SLMD BP Acne Spot Treatment, 10% Benzoyl Peroxide, 0.5 fl. oz - 15 mL bottles, Sandra Lee MD, Distributed by Skin PS Brands, Culver City, CA90232.

by Owen Biosciences Inc.

Reason: Chemical contamination: Presence of benzene
Published: April 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

HydroPeptide CLEAR ALLIANCE SERUM, 2.5% BENZOYL PEROXIDE, a)1 FL OZ/30ml; b) 2 FL OZ/60ml spray bottle; DIST BY HYDROPEPTIDE LLC, ISSAQUAH, WA 98027

by Owen Biosciences Inc.

Reason: Chemical contamination: Presence of benzene
Published: April 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

FHF Farmhouse Fresh, Midnight Clearing, NIGHT LOTION, 2.5% BENZOYL PEROXIDE ACNE TREATMENT, OTC a) 0.5 fl. oz./15ml; and b)1 fl. oz./30ml tubes; Made in the USA for FarmHouse Fresh, 8797 CR 858 McKinney, Texas

by Owen Biosciences Inc.

Reason: Chemical contamination: Presence of benzene
Published: April 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Cinacalcet Hydrochloride Tablets, 90 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-412-02

by Cipla USA, Inc.

Reason: CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit
Published: April 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Cinacalcet Hydrochloride Tablets, 60 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-411-02

by Cipla USA, Inc.

Reason: CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit
Published: April 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Cinacalcet Hydrochloride Tablets, 30 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-410-02

by Cipla USA, Inc.

Reason: CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit
Published: April 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1414-91.

by GE Healthcare Ireland Limited

Reason: Presence of particulate matter
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

GE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1413-63.

by GE Healthcare Ireland Limited

Reason: Presence of particulate matter
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Isotretinoin Capsules, USP, 40 mg, 10 count Prescription Pacs, Rx only, Manufactured for: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0591-2436-15 (carton), NDC 0591-2436-45 (blister pack).

by Teva Pharmaceuticals USA, Inc

Reason: Superpotent and Subpotent
Published: April 15, 2026
Distribution: FL, OH, PR & MS

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FDA Recall Ongoing 2026 recordClass II

Isotretinoin Capsules, USP, 30 mg, Rx Only, 10 count Prescription Pack, Manufactured for: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0591-2435-15 (carton), NDC 0591-2435-45 (blister pack).

by Teva Pharmaceuticals USA, Inc

Reason: Superpotent and Subpotent
Published: April 15, 2026
Distribution: FL, OH, PR & MS

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FDA Recall Ongoing 2026 recordClass II

Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: Viatris Specialty LLC, Morgantown, WV 06506, U.S.A, Made in Ireland, NDC 58151-506-91

by Viatris, Inc.

Reason: Failed Dissolution Specifications
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Artificial Tears Lubricant Eye Drops (glycerin 0.2%, hypromellose 0.2%, polyethylene glycol 400 1%), 0.5 oz bottles, Mfg: Geri-Care; Brooklyn, New York NDC 68788-7266-0

by Preferred Pharmaceuticals, Inc.

Reason: Lack of Assurance of Sterility
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Vancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5082-01

by Fagron Compounding Services

Reason: Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Vancomycin HCI, 1.5 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5085-01

by Fagron Compounding Services

Reason: Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Vancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5083-01

by Fagron Compounding Services

Reason: Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

norepinephrine Bitartrate, 32mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5027-02

by Fagron Compounding Services

Reason: Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

norepinephrine Bitartrate,16mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5026-02

by Fagron Compounding Services

Reason: Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Published: April 15, 2026
Distribution: Nationwide

View recall →

Data last updated: September 6, 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.