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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: SC ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 26, 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 I

NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (200 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-61.

by Advanced Pharma Inc.

Reason: Subpotent Drug: found to be below the specification for labeled assay.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj, USP QS 5 mL (200 mcg per mL), 5 mL Sterile single dose syringe, packaged in 8 x 5 (FORTY) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-67.

by Advanced Pharma Inc.

Reason: Subpotent Drug: found to be below the specification for labeled assay.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (100 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-818-61.

by Advanced Pharma Inc.

Reason: Subpotent Drug: found to be below the specification for labeled assay.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.25% Acetic Acid Irrigation USP, 500 mL Plastic Irrigation Container (PIC), B. Braun Medical Inc. Irvine CA 92614-5895 USA, NDC 0264-2304-10

by B. Braun Medical Inc

Reason: Presence of Particulate Matter: identified as polyethylene, which is consistent with the material used to manufacture the contain cap
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Methylphenidate Hydrochloride Extended-release Tablets, USP 54 mg, 100-count bottles, Rx Only, Trigen Laboratories, LLC. Bridgewater, NJ 08807, NDC 13811-709-10

by Osmotica Pharmaceutical Corp

Reason: Subpotent Drug
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Methylphenidate Hydrochloride Extended-release Tablets, USP 27 mg, 100-count bottles, Rx Only, Trigen Laboratories, LLC. Bridgewater, NJ 08807, NDC 13811-707-10

by Osmotica Pharmaceutical Corp

Reason: Subpotent Drug
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Riomet (metformin hydrochloride) Oral Solution Cherry Flavored 500 mg /5 mL, 4 fl. oz. (NDC 10631-206-01) and 16 fl. oz. (NDC 10631-206-02) HDPE bottles, Rx only, Manufactured for: Ranbaxy Laboratories Inc. Jacksonville, FL 32257 USA, Distributed by: Sun Pharmaceutical Industries, Cranbury, NJ 08512

by Sun Pharmaceutical Industries, Inc.

Reason: Microbial Contamination of Non-Sterile Products
Published: December 20, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Penicillin V Potassium for Oral Solution, USP, 125 mg (200,000 U) per 5 mL, 100 mL (when mixed) bottle, Rx only, Manufactured In Canada By: Teva Canada Limited, Toronto, Canada M1B 2K9; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454; NDC 0093-4125-73.

by Teva Pharmaceuticals USA

Reason: Failed Impurities/Degradation Specifications: high out of specification test results obtained for individual and total impurities.
Published: December 20, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

JLM Manufacturing LLC

Product: Dark Chocolate Almonds, Natural Dark Chocolate Almonds, 12/7…
Reason: JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
Published: December 20, 2017
Distribution: Sole customer is Lipari located in MI wh…

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FDA Recall United States Terminated Historical recordClass II

JLM Manufacturing LLC

Product: Natural Dark Chocolate Cranberries
Reason: JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
Published: December 20, 2017
Distribution: Sole customer is Lipari located in MI wh…

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FDA Recall United States Terminated Historical recordClass II

JLM Manufacturing LLC

Product: Dark Chocolate Almond Bark, 12/8oz.
Reason: JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
Published: December 20, 2017
Distribution: Sole customer is Lipari located in MI wh…

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FDA Recall United States Terminated Historical recordClass II

JLM Manufacturing LLC

Product: Dark Chocolate Raisins, Natural Dark Chocolate Raisins
Reason: JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
Published: December 20, 2017
Distribution: Sole customer is Lipari located in MI wh…

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FDA Recall United States Terminated Historical recordClass II

JLM Manufacturing LLC

Product: Dark Chocolate Coffee Beans, Natural Dark Chocolate Coffee B…
Reason: JLM Manufacturing LLC is recalling multiple dark chocolate products due to a supplier's recall for undeclared ingredient butterfat, and undeclared allergen milk.
Published: December 20, 2017
Distribution: Sole customer is Lipari located in MI wh…

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FDA Recall United States Terminated Historical recordClass III

Gourmet International Inc.

Product: Premio Strawberry Pralinati, Strawberry with Cocoa, 3.53oz,…
Reason: Gourmet International Inc. is initiating a voluntary recall of cookie products due to undeclared colors.
Published: December 20, 2017
Distribution: Domestic: Domestic only, no VA/DOD KY,…

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FDA Recall Terminated Historical recordClass I

grande X 5800 capsule, (Maca Root 120 mg, Horny Goat Weed 120 mg, Guarana Seed 80 mg, Ginko Leaf 60 mg, Saw Palmetto 100 mg, Damiana Leaf 100 mg, Ginseng Root 80 mg, Tribulus Terrestris 90 mg, Tongkat Alo 100 mg, Rhodiola Rosea 60 mg, L-Arginine 90 mg), 1-capsule packets, distributed by Grande X Ontario, CA 91745, UPC 640793555440

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

FIFTY SHADES 6000 capsule, Proprietary Raw Material 4550, 1-capsule packets, distributed by Express Pac Trading, UPC 4026666146056

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

PapaZen 3300 capsule, Proprietary Blend 1800mg, 1-capsule packets, distributed by FX Power San Diego, CA 92108, UPC 718122032587

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

RHINO 7 Platinum 5000, capsule, Proprietary Material: 750mg, 1-capsule packets, distributed by Fifty Shades Bayside, NY 11361, UPC 617135861224

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-925-16

by International Laboratories, Inc.

Reason: Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40 mg was filled with Bupropion hydrochloride XL Tablets 300 mg.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

The Kroger Co

Product: Comforts FOR BABY Purified Water with Flouride Added. 1 GAL…
Reason: the firm received a complaint of mold found in the product.
Published: December 13, 2017
Distribution: Product was shipped to the following sta…

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Data last updated: September 26, 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.