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Recall totals

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

37,204

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 30, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass I

Lipari Foods, Inc.

Product: Copper wood Colby Jack Mini Horn, 4/6#
Reason: Lipari Foods is recalling multiple cheeses because of a supplier's recall of cheese due to potential contamination with Listeria monocytogenes.
Published: April 5, 2017
Distribution: Domestic: Illinois, Indiana, Kentucky, M…

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FDA Recall United States Terminated Historical recordClass III

Give and Go Prepared Foods Corp - Finch

Product: The Bakery Mini Pecan Tarts Part Platter NET WT 16x 16.2 OZ…
Reason: Dried weevil larvae may be present in the recalled products.
Published: April 5, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Give and Go Prepared Foods Corp - Finch

Product: Two-Bite Pecan Tarts Party Platter 16 x 16.2 (460g) item num…
Reason: Dried weevil larvae may be present in the recalled products.
Published: April 5, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Give and Go Prepared Foods Corp - Finch

Product: Two-Bite Turtle Brownie Party Platter 16 x 12.2 oz (346g) it…
Reason: Dried weevil larvae may be present in the recalled products.
Published: April 5, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Give and Go Prepared Foods Corp - Finch

Product: Two-Bite Pecan Tart 9.2 oz (261g) item number 02023; NL Two-…
Reason: Dried weevil larvae may be present in the recalled products.
Published: April 5, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pinnacle Foods

Product: Buffalo Blue Kettle Cooked Potato Chips 8 oz (227g)
Reason: Snyder of Berlin is recalling their Buffalo Blue Kettle Cooked Potato Chips after being informed that a milk powder used within a spice blend ingredient may contain Salmonella.
Published: April 5, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

B & H Foods Inc

Product: Ruth's Cream Cheese w/Pineapple-Pecans, 12 oz. (UPC 74952-12…
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: April 5, 2017
Distribution: AL, GA, NC, SC, TN and VA.

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FDA Recall United States Terminated Historical recordClass I

B & H Foods Inc

Product: Ruth's Lite Pimento Spread, 12 oz. (UPC 74952-12000), Packed…
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: April 5, 2017
Distribution: AL, GA, NC, SC, TN and VA.

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FDA Recall United States Terminated Historical recordClass I

B & H Foods Inc

Product: Ruth's Jalapeno Pimento Spread, 12 oz. (UPC 74952-12014), Pa…
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: April 5, 2017
Distribution: AL, GA, NC, SC, TN and VA.

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FDA Recall United States Terminated Historical recordClass I

B & H Foods Inc

Product: Ruth's Old Fashion Pimento Spread, 16oz. (UPC 74952-15005),…
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: April 5, 2017
Distribution: AL, GA, NC, SC, TN and VA.

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FDA Recall United States Terminated Historical recordClass I

B & H Foods Inc

Product: Ruth's Original Pimento Spread 7oz (UPC 74952-0005), 12oz (…
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: April 5, 2017
Distribution: AL, GA, NC, SC, TN and VA.

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FDA Recall Terminated Historical recordClass II

Desonide Ointment, 0.05%, NET WT 60 grams tubes, Rx only, E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0309-60

by Fougera Pharmaceuticals Inc.

Reason: Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may contain tubes of Desonide Ointment labeled as Ketoconazole Cream
Published: March 29, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate Injection , USP, 200 mg/mL, 1 mL vial , For Intramuscular Use Only, Rx Only, Distributed by Sun Pharma Ind. Inc., NJ 08512, Manufactured by Sun Pharma Ind. Ltd. India, NDC 62756-015-40

by Sun Pharmaceutical Industries, Inc.

Reason: Presence of Particulate Matter
Published: March 29, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Famciclovir tablets, 500 mg, packaged in 30-count unit dose cartons, Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-307-13

by AVKARE Inc.

Reason: Failed impurities/ degradation specifications: Product was above specification for unknown impurities.
Published: March 29, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 900 mg/180 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-30).

by PFIZER INC

Reason: Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Published: March 29, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 750 mg/150 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-205-25).

by PFIZER INC

Reason: Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Published: March 29, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 300 mg/60 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-10).

by PFIZER INC

Reason: Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Published: March 29, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The Kroger Co., 1014 Vine Street, Cincinnati, OH 45202; Manufactured for: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045; NDC 68645-493-54.

by Legacy Pharmaceutical Packaging LLC

Reason: Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Published: March 29, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-023-10), Rx only, Manufactured by: Cadila Healthcare Ltd., India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534.

by Zydus Pharmaceuticals USA Inc

Reason: Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Published: March 29, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Country Fresh Inc.

Product: Southwestern Stuffed Mushrooms Net Wt. 7 oz. (199g) UPC: 072…
Reason: Possible contamination with Listeria monocytogenes.
Published: March 29, 2017
Distribution: Alabama, Florida, Georgia, Kentucky, Lou…

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Data last updated: September 30, 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.