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Recall totals

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

37,060

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/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 8, 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 Completed Historical recordClass II

Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-007-04

by Slate Run Pharmaceuticals

Reason: CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000-count bottle, Rx only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC 57237-018-99

by Rising Pharma Holding, Inc.

Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit.
Published: March 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Kids by babyganics SPF 50 mineral sunscreen totally tropical (titanium dioxide 3/5%, zinc oxide 7.25%), packaged in 3 OZ spray bottles, Dist. by KAS Direct LLC, 1525 Howe St. Racine, WI 53403, UPC 813277019923 and UPC 813277019916

by Johnson, S C and Son, Inc

Reason: Chemical Contamination
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Kids by babyganics SPF 50 totally tropical (titanium dioxide 3/5%, zinc oxide 7.25%) packaged in a) 6 OZ (170 g) spray bottles UPC 813277019954 and UPC 813277019800; and b) Twinpack UPC 813277019930; Dist. by KAS Direct LLC, 1525 Howe St. Racine, WI 53403.

by Johnson, S C and Son, Inc

Reason: Chemical Contamination
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Walgreens, Acne Control Cleanser, 10% Benzoyl Peroxide/Acne Treatment, NET WT 5 OZ (142g) Distributed by: Walgreen CO, 200 Wilmont RD, Deerfield, IL, Made in Canada. UPC#: 1 9560203602 8

by Sigan Industries Group Inc.

Reason: Chemical Contamination: Presence of benzene
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Zapzyt, Acne Treatment Gel, 10% benzoyl peroxide Gel, packaged in 1 oz (28.35g) tube, Distributed by: FOCUS CONSUMER HEALTHCARE, LLC., 801 Broad St Ste 200, Chattanooga, TN 37402. NDC 71687-0011-1

by Denison Pharmaceuticals, LLC

Reason: Chemical Contamination: Presence of benzene.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), Rx Only, CAPS, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, 855-275-2270, NDC 71285-6092-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Presence of Particulate Matter
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules, USP, 20mg, Rx Only, 500-count bottles, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-746-05

by Breckenridge Pharmaceutical, Inc.

Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, 1000-count bottles, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-747-10

by Breckenridge Pharmaceutical, Inc.

Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules, USP, 60mg, Rx Only, 1000-count bottles, Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceuticals, Inc., Berkeley Heights, NJ 07922. NDC 51991-748-10

by Breckenridge Pharmaceutical, Inc.

Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL, 100 mEq/L flexible container, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26; Bar Code (01)00309907074269

by ICU Medical, Inc.

Reason: Labeling: Label Error on Declared Strength. Overwrap labeled as Potassium Chloride Inj 10 mEq may contain flexible containers of Potassium Chloride Inj 20 mEq
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

POTASSIUM CHLORIDE Inj., 20 mEq total in 100 mL flexible container 24 x case, 200 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7075-26; Bar Code Flexible container (01) 00309907075266; Case (01)30309907075267

by ICU Medical, Inc.

Reason: Labeling: Label Error on Declared Strength. Cases labeled POTASSIUM CHLORIDE 20 mEq, may contain flexible containers with overwrap mislabeled as 10 mEq. The correct dosage strength of 20 mEq is printed on the labeling affixed to the product flexible container.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Unisom, SleepMelts, Diphenhydramine HCl tablets, 25 mg, Nighttime Sleep-Aid, 4 x 8 blister packs per carton, Cherry flavor, Manufactured by Adare Pharmaceuticals, Inc., Dist. by Chattem, Inc., P.O. Box 2219, Chattanooga, TN 37409, UPC # 0 41167 0014 0

by Chattem Inc

Reason: CGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the daily acceptable intake limit defined by the Food and Drug Administration.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

BD ChloraPrep Clear 1mL Applicators, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin Preparation, Sterile Solution, 0.03 fl. oz (1 mL) each, 60 Applicators per Carton, CareFusion 213, LLC, El Paso, TX 79912, Subsidiary of Becton, Dickinson and Co., REF 930480, NDC 54365-400-31.

by CareFusion 213, LLC

Reason: Non-Sterility: contamination of Aspergillus penicillioides, due to breach in package lidding.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sodium Chloride Injection 9%, USP, 500 mL, Single-Dose IV Bottle, Rx Only, nephron, 503B outsourcing facility, West Columbia, SC 29172, NDC: 69374-334-50

by Nephron Sterile Compounding Center LLC

Reason: Lack of Assurance of Sterility: There is a potential for leakage at the IV bottle port.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Chicken of the Sea; Thai Union

Product: Van Camp's branded Solid Light Yellowfin in Vegetable oil;…
Reason: Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Chicken of the Sea; Thai Union

Product: Trader Joe's branded Solid White Albacore Tuna in water, Low…
Reason: Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Chicken of the Sea; Thai Union

Product: Genova branded Yellowfin Tuna in Extra Virgin Olive Oil and…
Reason: Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Published: March 19, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Chicken of the Sea; Thai Union

Product: Trader Joe's branded Solid White Albacore Tuna in olive oil;…
Reason: Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Published: March 19, 2025
Distribution: Nationwide

View recall →

FDA Recall United States Ongoing Historical recordClass II

Chicken of the Sea; Thai Union

Product: Trader Joe's branded Solid Light Yellowfin Tuna in olive oil…
Reason: Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
Published: March 19, 2025
Distribution: Nationwide

View recall →

Data last updated: September 8, 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.