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Recall totals

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

37,341

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/haifa-smoked-fish-recalls-cold-smoked-sprats-due-potential-health-riskPublished October 27, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 28, 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	24,450
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 II

Venofer (iron sucrose) Injection, USP 100 mg Elemental Iron per 5 mL (20 mg/mL), 5 mL Single-Dose Vials, Rx Only, For Intravenous Use Only, American Regent, Inc. Shirley, NY 11967, NDC: 0517-2340-01 (vial), NDC: 0517-2340-10 (10 x 5 mL/vial cartons), NDC: 0517-2340-25 (25 x 5 mL/vial cartons).

by American Regent, Inc.

Reason: Presence of Particulate Matter: Potential for glass delamination from the vials.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Venofer (iron sucrose) Injection, USP 50 mg Elemental Iron per 2.5 mL (20 mg/mL), 2.5 mL Single-Dose Vials, Rx Only, For Intravenous Use Only, Distributed by: Fresenius Medical Care NA, Waltham, MA 02451, NDC: 49230-530-01 (vial), NDC: 49230-530-10 (10 x 2.5mL/vial cartons), NDC: 49230-530-25 (25 x 2.5mL/vial cartons).

by American Regent, Inc.

Reason: Presence of Particulate Matter: Potential for glass delamination from the vials.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Venofer (iron sucrose) Injection, USP 100 mg Elemental Iron per 5 mL (20 mg/mL), 5 mL Single-Dose Vials, Rx Only, For Intravenous Use Only, Distributed by: Fresenius Medical Care NA, Waltham, MA 02451, NDC: 49230-534-01 (vial), NDC: 49230-534-25 (25 x 5 mL/vial cartons).

by American Regent, Inc.

Reason: Presence of Particulate Matter: Potential for glass delamination from the vials.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Cinacalcet Tablets, 90 mg, packaged in: a) 30-count HDPE bottle (NDC 65862-833-30), b) 500-count HDPE bottle (NDC 65862-833-05), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India. 90 mg - 30 Tablets - NDC 65862-833-30 90 mg - 500 Tablets - NDC 65862-833-05

by Aurobindo Pharma USA Inc

Reason: cGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Cinacalcet Tablets, 60mg, packaged in: a) 30-count HDPE bottle (NDC 65862-832-30), b) 500-count HDPE bottle (NDC 65862-832-05), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India.

by Aurobindo Pharma USA Inc

Reason: cGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Cinacalcet Tablets, 30 mg, packaged in: a) 30-count HDPE bottle (NDC 65862-831-30); b) 500-count HDPE bottle (NDC 65862-831-05), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India.

by Aurobindo Pharma USA Inc

Reason: cGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-449-17

by ACCORD HEALTHCARE, INC.

Reason: Subpotent drug
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: December 31, 2024Historical recordClass I

Fresh Express Incorpated

Product: Fresh Express Gourmet Cafe Santa Fe Greek 5.2 oz, Labeled Sa…
Reason: Potential Listeria Monocytogenes Contamination. The pre-packaged condiment trays contains chicken linked to the Bruce Pac recall.
Published: December 11, 2024
Distribution: U.S. distribution within states in retai…

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FDA Recall United States TerminatedTerminated: December 31, 2024Historical recordClass I

Fresh Express Incorpated

Product: Fresh Express Gourmet Cafe Chicken Caesar 5.75oz, Labeled Sa…
Reason: Potential Listeria Monocytogenes Contamination. The pre-packaged condiment trays contains chicken linked to the Bruce Pac recall.
Published: December 11, 2024
Distribution: U.S. distribution within states in retai…

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FDA Recall United States TerminatedTerminated: May 6, 2025Historical recordClass I

HH FRESH TRADING CORP

Product: ENOKI MUSHROOM; 200g/package (25 packages/case); vacuum pack…
Reason: Potential contamination of Listeria monocytogenes
Published: December 11, 2024
Distribution: Retail stores in West Virginia.

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FDA Recall United States TerminatedTerminated: May 28, 2025Historical recordClass II

Cumberland Packing Corp.

Product: Organic Hot Agave in the Raw, 10 oz.
Reason: Elevated Osmophilic Yeast Count
Published: December 11, 2024
Distribution: Multiple states

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

Michael Zakany LLC

Product: Jose Madrid Salsa Chipotle Con Queso, Net Wt. 13 oz. (369g),…
Reason: Undeclared Yellow #5 and Yellow #6
Published: December 11, 2024
Distribution: Product was sold through 6 distributors…

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FDA Recall United States TerminatedTerminated: December 31, 2024Historical recordClass I

Albertsons Companies LLC

Product: (1) GINGER CHICKEN BROCCOLI SALAD FS (UPC 27110800000) (2) R…
Reason: Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes
Published: December 11, 2024
Distribution: AK, AZ, AR, CA, ID, IL, IN, IA, LA, ME,…

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FDA Recall United States TerminatedTerminated: December 31, 2024Historical recordClass II

Albertsons Companies LLC

Product: (1) READY MEALS CHICKEN STREET TACOS SS COLD (UPC 2713160000…
Reason: Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes
Published: December 11, 2024
Distribution: AK, AZ, AR, CA, ID, IL, IN, IA, LA, ME,…

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FDA Recall United States TerminatedTerminated: December 31, 2024Historical recordClass II

Albertsons Companies LLC

Product: (1) READY MEALS GREEN CHILI CHICKEN ENCHILADAS SS COLD (UPC…
Reason: Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes
Published: December 11, 2024
Distribution: AK, AZ, AR, CA, ID, IL, IN, IA, LA, ME,…

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FDA Recall United States TerminatedTerminated: February 4, 2025Historical recordClass II

Cedar's Mediterranean Foods, Inc.

Product: Member's Mark brand Roasted Red Pepper Hummus; 32 oz (907 g)…
Reason: Potential presence of foreign objects.
Published: December 11, 2024
Distribution: Multiple states

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FDA Recall TerminatedTerminated: September 16, 2025Historical recordClass II

Cooling Menthol Extra Strength Pain Relief Patch, Menthol 7.5%, packaged in box of 5, Distributed by J.R. Watkins LLC, Oakland CA 94612 UPC 8 56294 00878 5, NDC 72342-100-05

by JR Watkins

Reason: cGMP Deviations
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 16, 2025Historical recordClass II

PARCHE LEON PAIN RELIEVING HOT PATCH, Camphor 3%, Menthol 1.25%, Capsaicin 0.025%, 6 patches per box, Distributed by: Pharmadel LLC, Georgetown, DE 19947 NDC 55758-039-01, UPC 8 59424 00433 6

by Unexo Life Sciences Private Limited

Reason: cGMP Deviations
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 16, 2025Historical recordClass II

CHEEKY BONSAI PAIN RELIEF PATCHES, Menthol 10%, 4 patches per box, Distributed by Cheeky Bonsai, San Francisco, CA UPC 8 60006 57564 9

by Unexo Life Sciences Private Limited

Reason: cGMP Deviations
Published: December 4, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 16, 2025Historical recordClass II

JR WATKINS COOLING PAIN RELIEF PATCHES, Menthol 7.5%, 5 patches per box, Distributed By: J.R. Watkins, LLC, Oakland, CA 94612 UPC 8 56294 00878 5

by Unexo Life Sciences Private Limited

Reason: cGMP Deviations
Published: December 4, 2024
Distribution: Nationwide

View recall →

Data last updated: October 28, 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.