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Recall totals

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

37,343

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,860

Class I recallsReasonable probability of serious health consequences

24,450

Class II recallsTemporary or medically reversible health consequences

2,901

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 2,095 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vitality-works-inc-recalls-365-whole-foods-market-ashwagandha-capsules-sold-nationwide-due-potentialPublished October 30, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 30, 2026 ET

Summary (Year to date)

1,853 recalls have been announced year to date.
Oct 2026 was 45% lower than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).

Recalls by class

Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,450
Class I	9,860
Class III	2,901
Not Yet Classified	2

FDA Recall OngoingHistorical recordClass I

CVS Health brand, Lubricant Gel Drops (Carboxymethylcellulose Sodium 1%) packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 76168-704-15) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 76168-704-30), Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895.

by Kilitch Healthcare India Limited

Reason: Non-Sterility
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Leader brand Eye Irritation Relief (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline 0.05%), packaged in 0.5 FL OZ (15 mL) bottles, Cardinal Health Dublin, Ohio 43017, NDC 70000-0087-1

by Kilitch Healthcare India Limited

Reason: Non-Sterility
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

CVS brand Multi Action Relief Drops (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline 0.05%) packaged in 0.5 FL OZ (15mL) bottles, Distributed by CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895. NDC 76168-706-15

by Kilitch Healthcare India Limited

Reason: Non-Sterility
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Leader brand Dry Eye Relief (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%) packaged in 0.33 FL OZ (10 mL) bottles, Distributed by Cardinal Health Dublin, Ohio 43017, NDC 70000-0088-1

by Kilitch Healthcare India Limited

Reason: Non-Sterility
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

CVS Health brand Lubricating Gel Drops (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%), packaged in 0.33 FL OZ (10 mL) bottles, Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895. NDC 76168-712-10

by Kilitch Healthcare India Limited

Reason: Non-Sterility
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Rugby brand Polyvinyl Alcohol 1.4% Lubricating Eye Drops, packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rugby Laboratories, Livonia, MI 48152, NDC 0536-1325-94

by Kilitch Healthcare India Limited

Reason: Non-Sterility
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

CVS Health brand Lubricant Eye Drops (Propylene glycol 0.6%), packaged in a) 0.33 FL OZ (10mL) bottles (Single Pack) (NDC 76168-714-10) and b) 0.33 FL OZ (10 mL) bottles (Twin pack) (NDC 76168-714-20), Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895.

by Kilitch Healthcare India Limited

Reason: Non-Sterility
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Leader brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%), packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 70000-0090-1) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 70000-0090-2), Distributed by: Cardinal Health Dublin, Ohio 43017

by Kilitch Healthcare India Limited

Reason: Non-Sterility
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

CVS Health brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%), packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 76168-702-15) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 76168-702-30), Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895.

by Kilitch Healthcare India Limited

Reason: Non-Sterility
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 17, 2024Historical recordClass II

Omeza Skin Protectant, Skin Protectant Gel 10*2mL Vials

by OMEZA LLC

Reason: CGMP Deviations
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 17, 2024Historical recordClass II

Omeza Lidocaine Lavage pain relief oil 10*2mL VIALS

by OMEZA LLC

Reason: CGMP Deviations
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 22, 2024Historical recordClass II

Wegmans Food Markets, Inc.

Product: Ready To Bake Chocolate and Almond Variety Pk (UPC 87-85300-…
Reason: Product contains undeclared soy lecithin.
Published: February 14, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 22, 2024Historical recordClass II

Wegmans Food Markets, Inc.

Product: Ready To Bake Double Chocolate Croissant (UPC 87-85300-05006…
Reason: Product contains undeclared soy lecithin.
Published: February 14, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 22, 2024Historical recordClass II

Wegmans Food Markets, Inc.

Product: 24ct Petite Pastry Tray, plastic tray with white base and cl…
Reason: Product contains undeclared soy lecithin.
Published: February 14, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 22, 2024Historical recordClass II

Wegmans Food Markets, Inc.

Product: 9 oz 10pk Assorted Mini Danish, bakery box with clear top (U…
Reason: Product contains undeclared soy lecithin.
Published: February 14, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 22, 2024Historical recordClass II

Wegmans Food Markets, Inc.

Product: 5 oz 2pk Chocolate Croissant, bakery box with clear top (UPC…
Reason: Product contains undeclared soy lecithin.
Published: February 14, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: December 16, 2025Historical recordClass III

NOW Foods

Product: Protocol for Life Balance, Phosphatidyl Serine 300mg softgel…
Reason: Amount of Phosphatidyl Serine in product is less than stated on the label
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 19, 2025Historical recordClass I

MG Foods Middletown

Product: Authentic Fresh to You Deluxe Triple Decker Club Net Wt. 8.8…
Reason: Undeclared egg
Published: February 14, 2024
Distribution: Distributed to distributors in PA, NJ, M…

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FDA Recall United States TerminatedTerminated: March 1, 2024Historical recordClass II

County Fair Foods, Inc.

Product: Popcorn Pre-Pop in 8oz Polypropylene bag packaged 20 bags to…
Reason: Undeclared Yellow #5
Published: February 14, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 18, 2024Historical recordClass I

Zenzedi (Dextroamphetamine Sulfate) CII Tablets, USP, 30 mg, 30-count bottle, Rx only, Mfd. for: Arbor Pharmaceuticals, LLC., Atlanta, Georgia, 30328, NDC 24338-856-03

by Azurity Pharmaceuticals, Inc.

Reason: Labeling: Label Mix-up
Published: February 7, 2024
Distribution: Nationwide

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Data last updated: October 30, 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.