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Recall totals

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

37,269

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-raw-mild-cheddar-cheese-due-potential-e-coli-o157h7Published October 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 17, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall OngoingHistorical recordClass II

Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol and Arnica, Menthol 5%, 4.2 oz./120 g per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92121. NDC: 35192-020-02

by CA BOTANA International, Inc.

Reason: CGMP Deviations
Published: December 3, 2025
Distribution: Multiple states

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FDA Recall OngoingHistorical recordClass II

Sea Enzyme Ultra Umbrella Sunscreen SPF 30, Titanium Dioxide 4%, Octinoxate 4%, 4 oz./113.4 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-011-02

by CA BOTANA International, Inc.

Reason: CGMP Deviations
Published: December 3, 2025
Distribution: Multiple states

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FDA Recall OngoingHistorical recordClass II

Doctor D. Schwab Controlling Cream, Benzoyl Peroxide 2.7%, 1 FL OZ/ 30 ML per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92123. NDC: 35192-017-05

by CA BOTANA International, Inc.

Reason: CGMP Deviations
Published: December 3, 2025
Distribution: Multiple states

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FDA Recall OngoingHistorical recordClass II

Doctor D. Schwab Controlling Balm with Tea Tree Oil, Salicyclic Acid 0.8%, 1 FL OZ/ 30 ML per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92123. NDC: 35192-016-05

by CA BOTANA International, Inc.

Reason: CGMP Deviations
Published: December 3, 2025
Distribution: Multiple states

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FDA Recall OngoingHistorical recordClass II

Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50, Zinc Oxide 21%, 2.1 oz/61 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-043-17

by CA BOTANA International, Inc.

Reason: CGMP Deviations
Published: December 3, 2025
Distribution: Multiple states

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FDA Recall OngoingHistorical recordClass II

Doctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21%, 4 oz./ 113.4 g per tube, Manufactured by CA Botana, San Diego, CA 92123. NDC: 35192-042-02

by CA BOTANA International, Inc.

Reason: CGMP Deviations
Published: December 3, 2025
Distribution: Multiple states

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FDA Recall OngoingHistorical recordClass I

Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials, Rx only, Fresenius Kabi USA, LLC, NDC 63323-739-11 (unit of use), 63323-739-12 (unit of sale).

by Fresenius Kabi USA, LLC

Reason: Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Published: December 3, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01

by Medical Products Laboratories, Inc.

Reason: Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis
Published: December 3, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 6, 2026Historical recordClass II

Jeni's Splendid Ice Creams LLC

Product: Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89…
Reason: Undeclared allergens - wheat and soy
Published: December 3, 2025
Distribution: Multiple states

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FDA Recall United States OngoingHistorical recordClass II

Nats Nuts LLC

Product: Nat's Nuts Cinnamon Whiskey Pecans, 4 oz.
Reason: Contains undeclared cashews
Published: December 3, 2025
Distribution: Connecticut, New York, New Jersey, and N…

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FDA Recall OngoingHistorical recordClass I

POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL Flexible Container, Highly concentrated 100 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26

by Otsuka ICU Medical LLC

Reason: Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

POTASSIUM CHLORIDE Inj., 20 mEq total in 50 mL Flexible Container, Highly concentrated 400 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7077-14

by Otsuka ICU Medical LLC

Reason: Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl. oz.), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-266-04

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-107-34

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Renew Skin Repair Cream, Dimethicone 1.5%, packaged in a) 5g tube (NDC 61924-405-05), b) 4 oz tube (NDC 61924-405-04), and c) 800 mL (NDC 61924-405-27), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1%, 113g (4 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-435-04

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

PeriGiene, Health Care Antiseptic, Chloroxylenol 0.5%, 222mL (7.5 fl. oz.) bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

McKesson Skin Protectant, Lanolin USP, packaged in a) 5g (NDC 68599-6202-1), and b) 4oz NDC 68599-6203-4 tube, Distributed by McKesson Medical-Surgical Inc., Richmond, VA 23233.

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Lantiseptic, Skin Protectant, Lanolin USP 30%, packaged in a) 5g (0.17 oz) (NDC 61924-304-05), b)14.2g (0.5 oz)( NDC 61924-304-14), c) 4oz (NDC 61924-304-04), d) 4.5oz (NDC 61924-304-45), and e) 12oz (NDC 61924-304-12) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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Data last updated: October 17, 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.