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Recall totals

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

37,115

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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 2,072 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 16, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 9.8oz Chopped Teriyaki Pineapple Kit UPC:0-71430-00100…
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 9.1oz Peppercorn Ranch Chopped Kit UPC: 0-71430-00093…
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 8oz Shredded Lettuce UPC: 0-71430-01065-5 SKU: 2029
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 3lb Garden Salad UPC:0-71430-01138-6 SKU: 2163
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 24oz Value Size Garden Salad UPC:0-71430-01136-2 SKU:…
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 16oz Value Size Shredded Lettuce UPC:0-71430-84616-2…
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 13oz Southwest Kit UPC:0-71430-01701-2 SKU: 2776
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 13.25oz Country Ranch Kit UPC:0-71430-01730-2 SKU: 76…
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 12oz Garden Salad / Salade Du Jardin UPC:0-71430-01135…
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 12oz American UPC:0-71430-00933-8 SKU: 43
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 11oz Greener Selection UPC: 0-71430-01008-2 SKU: 34
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall United States Terminated Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole 10oz Very Veggie UPC: 0-71430-01008-2 SKU: 532
Reason: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole and found to contain Listeria monocytogenes.
Published: March 2, 2022
Distribution: Canada: AB, BC, NB, ON, QC, Sk; United S…

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FDA Recall Terminated Historical recordClass II

Erythromycin Topical Gel USP, 2%, Net Wt 30 g tube, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation, dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-053-66.

by Teligent Pharma, Inc.

Reason: Failed Impurities/Degradation Specifications: Lot not meeting specification for Unknown Max Related Compounds.
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

HCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj., For Sub-Q or IM Use Only, Not For IV Use, Vial, Rx Only, Compounded By: Revive Rx 3831 Golf Dr., Houston, TX 77018, NDC: 88888-1739-01.

by Revive Rx LLC dba Revive Rx Pharmacy

Reason: Non-sterility; bacterial contamination identified as Paenibacillus lautus.
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

PARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an insertion tube and solid white rod in a Tyvek polyethylene pouch, Rx Only, Manufactured by Teva Women's Health Inc. a subsidiary of Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 51285-204-01

by CooperSurgical, Inc

Reason: Non-sterility
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

RED MAMMOTH capsules, 400 mg, packaged in 10-count blisters per carton, ASIN B00KA8FBNI, barcode X001ANE0I5.

by Celebrate Today

Reason: Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

THE RED PILL, EXTRA STRENGTH capsules, 800 mg, packaged in 10-count blisters packaged in a carton, ASIN B0847BSQQ5, Barcode X002G5GMJ1.

by Your Favorite Shop

Reason: Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Chlorthalidone Tablets USP 25 mg, Rx Only, 100 Tablets, Sun Pharma, Mfg. by: Fontida Bio Pharm Inc., 1100 Orthodox St. Philadephia, PA 19124, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-648-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Foreign Matter identified as stainless steel microscopic wear particles mixed with punch lubricant oil and silicone particles from the dust cup
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Pyrazinamide Tablets, USP 500 mg, 100-count bottles, Rx only, Manufactured by: ULTRAtab Laboratories, Inc. Highland, NY 12528, Distributed by Par Pharmaceuticals, Chestnut Ridge, NY 10977, NDC 67253-660-10.

by ANI Pharmaceuticals, Inc.

Reason: cGMP Deviations
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprazolam Tablets, USP 2.0 mg, packaged in a) 100-count bottles (NDC 67253-903-10), b) 500-count bottles (NDC 67253-903-50), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977

by ANI Pharmaceuticals, Inc.

Reason: cGMP Deviations
Published: February 23, 2022
Distribution: Nationwide

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Data last updated: September 16, 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.