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Recall totals

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

37,497

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,881

Class I recallsReasonable probability of serious health consequences

24,543

Class II recallsTemporary or medically reversible health consequences

2,935

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 2,098 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-all-cheddar-cheese-products-because-possible-health-riskPublished November 10, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 11, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: August 15, 2017Historical recordClass I

Treehouse Foods

Product: UPC 041498205379, Southern Grove Tuscan Trail Mix, Best By/D…
Reason: TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published: October 12, 2016
Distribution: US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States TerminatedTerminated: August 15, 2017Historical recordClass I

Treehouse Foods

Product: UPC 041498211004, Southern Grove PB & Pretzel Trail Mix, Bes…
Reason: TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published: October 12, 2016
Distribution: US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States TerminatedTerminated: August 15, 2017Historical recordClass I

Treehouse Foods

Product: UPC 071725748010, Sunflower Seeds Roasted and Salted, Best…
Reason: TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published: October 12, 2016
Distribution: US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States TerminatedTerminated: August 15, 2017Historical recordClass I

Treehouse Foods

Product: UPC 4130300137, Essential Everyday Trail Mix Bars, Best By/…
Reason: TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published: October 12, 2016
Distribution: US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States TerminatedTerminated: August 15, 2017Historical recordClass I

Treehouse Foods

Product: UPC 071725711533, Natures Harvest Southwest Trail MixBest By…
Reason: TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published: October 12, 2016
Distribution: US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States TerminatedTerminated: August 15, 2017Historical recordClass I

Treehouse Foods

Product: UPC 071725714688, Raisin and Nut Trail Mix, Best By/Date Co…
Reason: TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published: October 12, 2016
Distribution: US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States TerminatedTerminated: August 15, 2017Historical recordClass I

Treehouse Foods

Product: UPC 071725728166, Natures Harvest Afternoon Snack Blend, Be…
Reason: TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published: October 12, 2016
Distribution: US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States TerminatedTerminated: August 15, 2017Historical recordClass I

Treehouse Foods

Product: UPC 070038614142, Best Choice Mountain Trail Mix, Best By/…
Reason: TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published: October 12, 2016
Distribution: US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall United States TerminatedTerminated: August 15, 2017Historical recordClass I

Treehouse Foods

Product: Sunflower Kernels packaged in the following brands and sizes…
Reason: TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.
Published: October 12, 2016
Distribution: US: AL, AZ, AR, CA, CO, CT, FL, IL, IN,…

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FDA Recall TerminatedTerminated: May 3, 2017Historical recordClass III

Lansoprazole Delayed-Release Capsules, USP, 30 mg, packaged in 100-count cartons of 10 x 10 unit dose blister cards, Rx only, Manufactured by: Dr. Reddy's Laboratories, Inc., 200 Somerset Corporate Blvd Floor 7, Bridgewater, NJ 08807, NDC 63739-0555-10

by Mckesson Packaging Services

Reason: Labeling: Label mix-up. The inner packaging was properly labeled Omeprazole DR 40mg Capsules, but the outer secondary packaging was mislabeled Lansoprazole Delayed-Release 30mg Capsules.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 9, 2017Historical recordClass III

PREMARIN (conjugated estrogen tablets, USP) 1.25 mg, 1000- count bottle, Rx only, Distributed by: Wyeth Pharmaceuticals Inc. A subsidiary of Pfizer Inc. Philadelphia, PA 19101, NDC 0046-1104-91

by Pfizer Inc.

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: Bottles were incorrectly labeled with an expiry date of 11/17; the correct date is 09/17.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 23, 2024Historical recordClass II

Senna Syrup (sennosides) 8.8 mg, 8 fl. oz. (237 mL) bottle, Distributed by: Major Pharmaceuticals, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0904-6289-09.

by Pharmatech LLC

Reason: CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 23, 2024Historical recordClass II

Senexon Liquid (sennosides) 8.8 mg, 8 fl oz. (237 mL) bottle, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1000-59.

by Pharmatech LLC

Reason: CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 23, 2024Historical recordClass II

Diocto Syrup (docusate sodium), 60 mg/15 mL, One Pint (473 mL) bottle, Dist. by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1001-85.

by Pharmatech LLC

Reason: CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 23, 2024Historical recordClass II

Aller-Chlor (chlorpheniramine maleate) Syrup, USP, 2 mg in each 5 mL, 4 fl oz (120 mL) bottle, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1025-47.

by Pharmatech LLC

Reason: CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 23, 2024Historical recordClass II

Ninjacof-A (acetaminophen, chlophedianol HCl, pyrilamine maleate) Liquid, 160 mg/12.5 mg/12.5 mg in each 5 mL, 16 fl oz (473 mL) bottle, Manufactured for: Centurion Labs, LLC, Birmingham, AL 35243, NDC 23359-033-16.

by Pharmatech LLC

Reason: CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 23, 2024Historical recordClass II

Ninjacof (chlophedianol HCl and pyrilamine maleate) Liquid, 12.5 mg/12.5 mg in each 5 mL, 16 fl oz (473 mL) bottle, Manufactured for: Centurion Labs, LLC, Birmingham, AL 35243, NDC 23359-032-16.

by Pharmatech LLC

Reason: CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 23, 2024Historical recordClass II

Sennazon (sennosides) Syrup, 8.8 mg, 8 fl. oz. (237 mL) bottle, Mfd. for: Bayshore Pharmaceuticals, Tampla, FL 33619, NDC 76518-100-08.

by Pharmatech LLC

Reason: CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 7, 2017Historical recordClass III

Lamotrigine Tablets, USP, 150 mg, 500-count Tablets per bottle, Rx only, Manufactured by: Unichem Laboratories LTD., Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511 India; Marketed by: Unichem Pharmaceuticals (USA), Inc ., Rochelle Park, NJ 07662; NDC 29300-113-05.

by UNICHEM PHARMACEUTICALS USA INC

Reason: Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the tablets.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 3, 2016Historical recordClass I

Bounce Life Style HQ

Product: Bounce Energy Ball Cashew & Pecan Vitality Lift, each loose…
Reason: Bounce Energy Ball Cashew & Pecan Vitality Lift is recalled because it has the potential to be contaminated with Listeria monocytogenes. This product contains sunflower kernels that were recalled by supplier SunOpta.
Published: October 5, 2016
Distribution: Nationwide

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Data last updated: November 11, 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.