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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 28, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Ritussin DM Dextromethorphan Hydrobormide (Dextromethorphan HBr, USP 10 mg, Guaifenesin, USP 100mg), packaged in 4 FL.OZ. (118 mL), RIJ PHARMACEUTICAL CORPORATION 40 COMMERCIAL AVENUE, MIDDLETOWN, NY 10941, NDC 5380740904, UPC 35380740941

by RIJ Pharmaceutical LLC

Reason: CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published: June 20, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

GeriCare Senna Syrup (Sennosides 8.8 mg), 8 fl oz (237 mL) bottles, Dist, by Gericare Pharmaceuticals 1650 63rd Street Brooklyn, NY 11204, NDC 57696-452-08, UPC 357896452087

by RIJ Pharmaceutical LLC

Reason: CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published: June 20, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

RPC APAP Elixir (Acetaminophen 160mg), Packaged in 16 FL. OZ. (473 mL) bottles, RIJ PHARMACEUTICAL CORPORATION, 40 COMMERCIAL AVENUE, MIDDLETOWN, NY, NDC 53807-129-16, UPC 353807129161

by RIJ Pharmaceutical LLC

Reason: CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published: June 20, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Gericare Liquid Pain Relief Acetaminophen Cherry Flavor 160mg/5mL, packaged in 16 FL OZ (473 mL), Dist. By Gericare Pharmaceuticals 1650 63rd Street Brooklyn, NY 11204, NDC 5789618016, UPC 357896180164

by RIJ Pharmaceutical LLC

Reason: CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published: June 20, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

RPC Children's Non-Aspirin (Acetaminophen 160 mg) Elixir, packaged in 4 FL. OZ. (118 mL), RIJ PHARMACETUICAL CORPORATION, 40 COMMERCIAL AVENUE, MIDDLETOWN, NY 10941, NDC 53807-129-04, UPC 353807129048

by RIJ Pharmaceutical LLC

Reason: CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published: June 20, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

RPC Senna Syrup (Sennosides 8.8mg), packaged in 8 fl oz (237 mL) bottles, RIJ Pharmaceuticals Corporation 40 Commercial Avenue, Middletown, NJ 10941, NDC 5380755608, UPC 353807556080

by RIJ Pharmaceutical LLC

Reason: CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published: June 20, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Preferred Plus Pharmacy Antacid (Aluminum Hydroxide 200mg, Magnesium Hydroxide 200mg Simethicone 20mg, packaged in 12 FL. OZ. (355 mL) bottles, Manufactured By: RIJ PHARMACEUTICAL CORPORATION 40 Commercial Avenue Middletown, NY 10941, Distributed by: Kinray Inc. Whitestone, NY 11357, NDC 53807-12612, UPC 53807126122

by RIJ Pharmaceutical LLC

Reason: CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published: June 20, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Preferred Plus Pharmacy Antacid Extra Strength (Aluminum Hydroxide 400mg, Magnesium Hydroxide 400mg, Simethicone 40 mg), packaged in 12 FL. OZ. (355 mL), Manufactured By: RIJ Pharmaceutical Corp.40 Commercial Avenue, Middletown, NY 10941, Distributed by: Kinray Inc. Whitestone, NY 11357 NDC 53807-158-12, UPC 353807158123

by RIJ Pharmaceutical LLC

Reason: CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Published: June 20, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Divvies LLC

Product: simply delicious Divvies SEMI-SWEET PEPPERMINT BARS made to…
Reason: Product may contain traces of milk.
Published: June 20, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

New Century Snacks LLC

Product: Snak Club Tropical Trail Mix: 16 oz. plastic pouch: Ingr…
Reason: Firm was notified by customer that some bags of Tropical Trail mix contain Yogurt Trail mix and therefore do not declare milk, soy, wheat or cashews.
Published: June 20, 2018
Distribution: Alabama, Arizona, California, Colorado,…

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FDA Recall Terminated Historical recordClass I

Naloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL Carpuject Single-use cartridge syringe, Single unit (NDC 0409-1782-03) and 10 count box (NDC 0409-1782-69), Rx Only, Hospira Inc., Lake Forest, IL

by HOSPIRA INC, LAKE FOREST

Reason: Presence of Particulate Matter; Potential for particulate matter on the syringe plunger.
Published: June 13, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Nystatin Oral Suspension, USP, 500,000 units/5 mL, For Institutional Use Only, packaged in 5 mL cups, Rx Only, Pharmaceutical Associates, Inc. Greenville, SC 29605, NDC 0121-4810-05

by Pharmaceutical Associates Inc

Reason: Resuspension problems: Out of specification for appearance and resuspendability.
Published: June 13, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Fluticasone propionate Nasal Spray, USP, 50 mcg, packaged in 50 mcg per spray 120 Metered Sprays bottles, 16 g net fill weight, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, FL 33326, NDC 60505-0829-1

by Apotex Inc.

Reason: Presence of foreign substance: glass particles
Published: June 13, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Desly International Corp.

Product: Melanie Mini Cookies with Caramel Flavor in a 17.6 oz (500g)…
Reason: Products contain undeclared peanuts.
Published: June 13, 2018
Distribution: CA CT FL GA IL KS KY MA MD ME…

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FDA Recall United States Terminated Historical recordClass I

Desly International Corp.

Product: Melanie Liubitelskie Cookies in a 17.6 oz (500g) clear plast…
Reason: Products contain undeclared peanuts.
Published: June 13, 2018
Distribution: CA CT FL GA IL KS KY MA MD ME…

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FDA Recall United States Terminated Historical recordClass I

GLOBAL COMMODITIES INC

Product: WATAN DRY FRUITS PREMIUM QUALITY NATURAL DRIED APRICOT WITH…
Reason: Product contains high levels of undeclared sulfites (2901 ppm).
Published: June 13, 2018
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

BLM Products U. Vertriebsges

Product: Priano Rosso Pesto Sauce, 6.7oz glass jar
Reason: BLM Prod.-und Vertriebsges.mbH & Co. KG has initiated a voluntary recall of Priano Rosso Pesto Sauce, 6.7 oz. packaged in glass jars due to undeclared allergens egg and milk.
Published: June 13, 2018
Distribution: Domestic only: Arkansas, California, Con…

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FDA Recall United States Terminated Historical recordClass II

Dean Foods, Inc.

Product: Baskin Robbins Mint Chocolate Chip
Reason: Product may contain unlabeled coconut.
Published: June 13, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Lake Michigan Distilling Co LLC

Product: Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, M…
Reason: Lake Michigan Distilling, LLC, dba Ethanol Extraction has initiated a voluntary recall of Ethanol Extraction s 190 Proof Non-Denatured Grain Alcohol due to contamination with methanol which could cause serious injury or death if consumed.
Published: June 13, 2018
Distribution: Domestic: AK, AL, AR, AZ, CA, CO, CT, DC…

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FDA Recall United States Terminated Historical recordClass II

The C.F. Sauer Company

Product: Code - Red Pepper Seasoning (21 oz.) Net Weight: 21 oz., N…
Reason: The C.F. Sauer Company has decided to initiate a recall of the following products: 1) Sauer - Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R, 18031R, 17306R, 17219R, 17135R, 17086R, 16322R, 16251R, 16238R, 16181R, 16068R, 15357R, 15328R, 15252R, 15174R, 15127R and 15125R. 2) Blue Mountain Valley - Red Pepper Seasoning (21 oz.) with the following lot codes: 18031R, 17306R, 17219R, 17205R, 17135R, 17086R, 16322R, 16243R, 16068R and 15357R. 3) Pocahontas - Red Pepper Seasoning (21 oz.) with the following lot codes: 17219R, 17135R and 15174R. 4) Premium - Recipe Red Pepper Seasoning (21 oz.) with the following lot codes: 18107R and 18072R. 5) Code - Red Pepper Seasoning (21 oz.) with the following lot codes: 17205R The C.F. Sauer Company recalled the products due to Milk allergen not being listed in the ingredient statement or in a separate allergen statement. Undeclared allergen.
Published: June 13, 2018
Distribution: Product has been distributed to: Georgia…

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Data last updated: September 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.