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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 United States Ongoing2026 recordClass III

Fazt & Loud LLC

Product: Lost and Found Energy, Sour Gummy Bear, 12pck, 16oz Cans Cas…
Reason: Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine, instead of 150mg as provided on the can.
Published: February 11, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass III

Glycopyrrolate Oral Solution, 1 mg/5 mL, 16 oz. (473 mL), Rx only, Manufactured by: MSN Pharmaceuticals Inc., Piscataway, NJ 08854, Distributed by: Novadoz Pharmaceuticals LLC, Piscataway, NJ 08854, NDC 72205-070-72

by NOVADOZ PHARMACEUTICALS LLC

Reason: Failed Impurities/Degradation Specifications
Published: February 4, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton containing 21 Tablets, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977. NDC 59762-4440-2

by Greenstone Llc

Reason: Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information when following the directions on the foil.
Published: February 4, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass III

parodontax (cetylpyridinium chloride)ACTIVE GUM HEALTH, Mouthwash, Mint. Net Wt 16.9 FL OZ (500 mL), Distributed by Haleon, Warren, NJ 07059. NDC 0135-0651-02

by Haleon US Holdings LLC

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles.
Published: February 4, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Sterile Water for Irrigation, 250 mL, Single-Dose Plastic Bottle, Rx Only, Baxter Healthcare Corporation Deerfield, IL 60015 NDC: 0338-0004-02.

by Baxter Healthcare Corporation

Reason: Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution
Published: February 4, 2026
Distribution: Nationwide

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FDA Recall United States Completed2026 recordClass I

SUPERFOODS, INC.

Product: a.) Live it Up brand Super Greens; Natural Wild Berry Flavor…
Reason: Products may be contaminated with Salmonella Typhimurium
Published: February 4, 2026
Distribution: Nationwide

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FDA Recall United States Completed2026 recordClass I

SUPERFOODS, INC.

Product: Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgr…
Reason: Products may be contaminated with Salmonella Typhimurium
Published: February 4, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing2026 recordClass II

QUTEN RESEARCH INSTITIUTE LLC

Product: Qunol, Extra Strength Turmeric Capsule, 1000mg ,HDPE bottle…
Reason: Mold contamination detected for raw material lots that were produced in July and used in finished goods.
Published: February 4, 2026
Distribution: The product was distributed to the follo…

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FDA Recall Ongoing2026 recordClass II

Icosapent Ethyl capsules, 1 gram, 120-count bottles, Rx only, Manufactured by: Softgel Healthcare Pvt. Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1592-07

by Zydus Pharmaceuticals (USA) Inc

Reason: Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsules
Published: January 28, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Thyroid, USP, Rx only, Net Wt: 0.50kg, For Manufacturing, Processing or Repackaging Use Only, Specialty Process Labs, Phoenix, AZ 85034, NDC 81305-100-02

by Specialty Process Labs LLC

Reason: Subpotent Drug
Published: January 28, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Furosemide Tablets, USP 40 mg, 1,000 Tablets, Rx Only, Manufactured for: Rising Pharmaceuticals Inc., East Brunswick, NJ 08816, Manufactured by: Graviti Pharmaceuticals Pvt. Ltd. Telangana - 502307, India, NDC 64980-563-10.

by Graviti Pharmaceuticals Private Limited

Reason: Presence of Foreign Substance
Published: January 28, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass III

Diclofenac Sodium Topical Gel, 1%, NET WT 100 g (3.53 oz), Manufactured by: DPT Laboratories, Ltd., 307 E Josephine Street, San Antonio, TX 78215. NDC: 76282-103-39

by Cipla USA, Inc.

Reason: Failed PH Specifications
Published: January 28, 2026
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: May 11, 20262026 recordClass II

Lily's Bakery Factory

Product: Cuban Crackers Galletas Cubanas, Net Wt 8Oz (226g). Distribu…
Reason: Undeclared colors FD&C yellow #5, FD&C yellow #6, and FD&C red 40
Published: January 28, 2026
Distribution: Product was only distributed in Florida.

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FDA Recall United States TerminatedTerminated: May 27, 20262026 recordClass II

CATAO MARKET LLC

Product: Mini Gaceniga Authentic Cuban Loaf Cake Classic (Net Wt. 12…
Reason: Undeclared colors FD&C Yellow #5
Published: January 28, 2026
Distribution: Product distributed only in FL.

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FDA Recall United States TerminatedTerminated: May 27, 20262026 recordClass II

CATAO MARKET LLC

Product: Mini Gaceniga Authentic Cuban Loaf Cake Raisins (Net Wt. 12…
Reason: Undeclared colors FD&C Yellow #5
Published: January 28, 2026
Distribution: Product distributed only in FL.

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FDA Recall United States TerminatedTerminated: May 27, 20262026 recordClass II

CATAO MARKET LLC

Product: Gaceniga Authentic Cuban Loaf Cake Raisins (Net Wt. 24 oz (6…
Reason: Undeclared colors FD&C Yellow #5
Published: January 28, 2026
Distribution: Product distributed only in FL.

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FDA Recall United States TerminatedTerminated: May 27, 20262026 recordClass II

CATAO MARKET LLC

Product: Gacen¿iga Authentic Cuban Loaf Cake Classic (Net Wt. 24 oz (…
Reason: Undeclared colors FD&C Yellow #5
Published: January 28, 2026
Distribution: Product distributed only in FL.

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FDA Recall Ongoing2026 recordClass II

Lanreotide Injection, 120 mg/0.5 mL, 0.5 mL per pre-filled syringe, For deep subcutaneous injection, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-870-67

by Cipla USA, Inc.

Reason: Presence of Particulate Matter.
Published: January 21, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Toothpaste: a) COLGATE, TOOTHPASTE, WHITENING, 2.5oz, 24ct; UPC: 035000511065; b) COLGATE, TOOTHPASTE, Regular, 2.5oz, 24ct, UPC: 035000511058; c) COLGATE, TOOTHPASTE, TRIPLE, 2.5oz, 24ct, UPC: 035000512109; d) COLGATE, TOOTHPASTE, MINT ZING, 24CT, 2.5oz, UPC: 035000744609; COLGATE, MAXFRESH, SPICY FRESH, RED TOOTH PASTE, 72CT, 150G; e) CREST, TOOTHPASTE, 40CT, 8.2OZ, UPC: 037000247081

by GOLD STAR DISTRIBUTION INC

Reason: CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Published: January 21, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Deodorant: a) Axe, Body Spray, Wild Spice, 6CT, 150ML, UPC: 600108736469; b) LUCKY MENS STICK DEODORANT, SPRING FRESH, 24CT, 2.5 OZ, UPC: 808829111668; c) LUCKY MENS STICK DEODORANT, FRESH COMFORT, 24CT, 1.6 OZ, UPC: 808829089103; d) LADY DEODORANT, CHERRY BLOSSOSM, 24CT, 1.8oz, UPC: 048155921092; e) AXE, BODY SPRAY, APOLLO, 6CT, 150ML; f) AXE, BODY SPRAY, BLACK, 6CT, 150ML; g) AXE, BODY SPRAY, DARK TEMPTATION, 6CT, 150ML; h) AXE, BODY SPRAY, GOLD, 6CT, 150ML; i) AXE, BODY SPRAY, EXCITE, 6CT, 150ML; j) AXE, BODY SPRAY, ICE CHILL, 6CT, 150ML; k) AXE, BODY SPRAY, MUSK, 6CT, 150ML; l) AXE, DEODORANT SPRAY, ADRENALIN, 6CT, 150ML

by GOLD STAR DISTRIBUTION INC

Reason: CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Published: January 21, 2026
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.