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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 18, 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

boardwalk ANTIBACTERIAL HANDSOAP REFILL, Chloroxylenol 0.1%, 1 gal. (3.78 L), Manufactured for Essendant Co., One Parkway North, Deerfield, IL 60015

by Midlab Incorporated

Reason: cGMP Deviations: Out of specification results for micro in hand soap products.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

MAXIM Assure Antibacterial, Chloroxylenol 0.1%, Net Contents: One U.S. Gallon (3.78 L), For Industrial and Institutional Use Only, MIDLAB 140 Private Brand Way, Athens, TN 37303

by Midlab Incorporated

Reason: cGMP Deviations: Out of specification results for micro in hand soap products.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

ZapMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZapMax, 2108 N St. Sacramento, CA 95816, www.zapmax.com

by Boulla LLC

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

ZoomMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZoomMax, 2108 N St. Sacramento, CA 95816, www.zoommax.com

by Boulla LLC

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

PeakMax Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: PeakMax, San Francisco, CA, www.PeakMax.com

by Boulla LLC

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
Published: December 11, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

VitalityXtra Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: VitalityXtra, San Francisco, CA www.vitalityxtra.com

by Boulla LLC

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
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, 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: 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: 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 United States CompletedHistorical recordClass II

DYMA BRANDS

Product: MONARCH INSTANT CHOCOLATE PUDDING & PIE FILLING MIX NATURALL…
Reason: After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
Published: December 11, 2024
Distribution: Products were distributed to the followi…

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FDA Recall United States CompletedHistorical recordClass II

DYMA BRANDS

Product: THIRSTER LOW CAL FRUIT, NET WT. 8.6OZ, Case UPC 507581083973…
Reason: After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
Published: December 11, 2024
Distribution: Products were distributed to the followi…

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FDA Recall United States CompletedHistorical recordClass II

DYMA BRANDS

Product: THIRSTER Lemonade Drink Mix NATURALLY FLAVORED LOW CALORIE,…
Reason: After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
Published: December 11, 2024
Distribution: Products were distributed to the followi…

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Data last updated: October 18, 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.