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Recall totals

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

37,271

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 recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 19, 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

Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Tube, NET WT 4oz (113.39g), painwizard.com Made in the USA, PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00019 2

by ARG Laboratories, Inc.

Reason: Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Tube, NET WT 8 oz (226.79g), Made in the USA, painwizard.com PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00011 6

by ARG Laboratories, Inc.

Reason: Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

ALOE GATOR, (Octocrylene 8%, Octyl Methoxycinnamate 6%, Benzophone 3 6%, Octyl Salicylate 5%), Original Formula, SPF 40+, Broad Spectrum Protective Gel, Sport Performance, NET WT 1 OZ (28 g), Manufactured for AGS Brands.

by ARG Laboratories, Inc.

Reason: Out of Specification for active ingredient
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Bull Frog SPF 50 Amphibious Lotion SPF 50 Amphibious Lotion with Water Armor Tech, Broad Spectrum Sunscreen with UVA/UVB Protection, NEW WT. 5 FL OZ (148ML), Distributed by: Bullfrog Brands LLC, PO Box 600207, Dallas, TX 75360 USA. UPC 8 50016 52112 5

by ARG Laboratories, Inc.

Reason: Out of Specification for active ingredient
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

NATURAL PAIN RELIEVING CREAM, GOLDEN TIGER, (Camphor 3%, Menthol 3%) Enriched with Capsaicin, Aloe Vera, Willow Bark & MSM, Gallon Jug 128 fl. oz. (3776 ml), Manufactured for Golden Tiger LLC, Made in USA, UPC 1 82294 00005 5

by ARG Laboratories, Inc.

Reason: Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM, Bottle with pump, NET WT 16 fluid oz / 473.17 ml, Made in USA, www.painwizard.com Pain Wizard LLC.PO Box 1099, Johnstown, CO 80534, UPC 8 63865 00012 3

by ARG Laboratories, Inc.

Reason: Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free 1mL Single-Use vial for Intraocular Injection, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-640-01

by Imprimis NJOF, LLC

Reason: Lack of Assurance of Sterility
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 29, 2025Historical recordClass II

Cefdinir for Oral Suspension USP, 250 mg/5 mL, packaged in a 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, Manufactured by: Lupin Limited, Mandideep, 462 046 India, NDC 68180-723-04

by Lupin Pharmaceuticals Inc.

Reason: Defective container: lack of seal integrity.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Metoprolol Tartrate Tablets USP, 25mg, 1000 count bottle, Rx only, distributed by: TruPharma, LLC, Tampa, FL 33609, Manufactured by: Rubicon Research Private Limited, Ambernath Dist Thane 421506 India, NDC 52817-360-00

by Rubicon Research Private Limited

Reason: Presence of Foreign Substance: metal in tablet
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Moxifloxacin 4 mg/0.8 mL Preservative-Free 0.8mL Single-Use vials for Intraocular Injection, Rx only, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-511-08

by Imprimis NJOF, LLC

Reason: Lack of Assurance of Sterility
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Moxifloxacin 0.8 mg/0.8 mL Preservative-Free 0.8mL Single-Use vials for Intraocular Injection, Rx only, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-509-08

by Imprimis NJOF, LLC

Reason: Lack of Assurance of Sterility
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Dexamethasone-Moxifloxacin- Ketorolac (1mg/mL, 0.5 mg/mL and 0.4 mg/mL), Preservative-Free, 1mL Single-Use vials for Intraocular Injection, Rx only, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-513-01

by Imprimis NJOF, LLC

Reason: Lack of Assurance of Sterility
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Dexamethasone-Moxifloxacin (1 mg/mL and 5mg/mL) Preservative-Free, 1mL Single-Use vials for Intraocular Injection, Rx only, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-512-01

by Imprimis NJOF, LLC

Reason: Lack of Assurance of Sterility
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free 1mL Single-Use vials for Intraocular Injection, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-640-01

by Imprimis NJOF, LLC

Reason: Lack of Assurance of Sterility
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Tirzepatide 10 mg/0.5 mL Sterile Solution, 2 mL Multi-dose vial, Rx only, This is a Compounded Product By: Revive RX Pharmacy, 3831 Golf Dr A, Houston, TX 77018, internally assigned NDC 99000-9278-64

by Revive Rx LLC dba Revive Rx Pharmacy

Reason: Labeling: Label Mix-up - product labeled as tirzepatide contains testosterone cypionate
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Zoledronic Acid Injection 5mg/100mL Sterile Solution, 100mL Single-Dose vials, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-688-52

by Dr. Reddy's Laboratories, Inc.

Reason: Lack of Assurance of Sterility: Leaking vials
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 11, 2025Historical recordClass II

Cathflo activase (ALTEPLASE), 2mg vials, Rx only, Genentech Inc., South San Francisco, CA 94080, NDC 50242-041-64

by Genentech, Inc.

Reason: Lack of Assurance of Sterility: Deformed stoppers observed during filling operations for Cathflo Activase.
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 28, 2024Historical recordClass I

Hy-Vee Stores Inc

Product: Hy-Vee To Go Cookies & Cream Mix, Net wt. 4 oz (113g), UPC 0…
Reason: Potential Salmonella contamination
Published: June 5, 2024
Distribution: Multiple states

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FDA Recall United States OngoingHistorical recordClass II

Nutrition Corp

Product: Fresh N Lean brand Crustless Chicken Potato Pot Pie. Package…
Reason: Possible contamination with Listeria monocytogenes
Published: June 5, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass II

Maribel's Sweets, Inc.

Product: 9. 25pc Mother s Day heart ganache box
Reason: Contains undeclared coconut.
Published: June 5, 2024
Distribution: Nationwide

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Data last updated: October 19, 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.