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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

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
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 11,821–11,840 of 19,566 recalls

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

View recall →

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

View recall →

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

View recall →

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

View recall →

FDA Recall United States Terminated Historical recordClass II

Raley's

Product
Raley's All Butter Meyer Lemon Cookie; Case of Raw Dough (1…
Reason
Plastic material was found in unbaked Meyer Lemon Cookies at retail store.
Published
December 27, 2017
Distribution
CA and NV

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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

First Source, LLC

Product
(Canada) Circle K Favourites Dark Chocolate Covered Almonds…
Reason
Chocolate products contain undeclared milk
Published
December 20, 2017
Distribution
AR, AZ, CA, CO, FL, GA, IL, KY, LA, MA,…

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FDA Recall United States Terminated Historical recordClass II

First Source, LLC

Product
(Canada) - Favourites Dark Chocolate Covered Almonds 113 gra…
Reason
Chocolate products contain undeclared milk
Published
December 20, 2017
Distribution
AR, AZ, CA, CO, FL, GA, IL, KY, LA, MA,…

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FDA Recall United States Terminated Historical recordClass II

First Source, LLC

Product
Tops Dark Chocolate Coffee Beans Net Wt 12 OZ (340g) UPC: 0…
Reason
Chocolate products contain undeclared milk
Published
December 20, 2017
Distribution
AR, AZ, CA, CO, FL, GA, IL, KY, LA, MA,…

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FDA Recall United States Terminated Historical recordClass II

First Source, LLC

Product
Wegmans Dark Chocolate Strawberries 13.5oz (383g) tub, UPC:…
Reason
Chocolate products contain undeclared milk
Published
December 20, 2017
Distribution
AR, AZ, CA, CO, FL, GA, IL, KY, LA, MA,…

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FDA Recall United States Terminated Historical recordClass II

First Source, LLC

Product
Wegmans Dark Chocolate Cherry Infused Cranberries 12 OZ (340…
Reason
Chocolate products contain undeclared milk
Published
December 20, 2017
Distribution
AR, AZ, CA, CO, FL, GA, IL, KY, LA, MA,…

View recall →

FDA Recall United States Terminated Historical recordClass II

First Source, LLC

Product
(1)Wegmans Dark Chocolate Almonds with Sea Salt and Turbinad…
Reason
Chocolate products contain undeclared milk
Published
December 20, 2017
Distribution
AR, AZ, CA, CO, FL, GA, IL, KY, LA, MA,…

View recall →

FDA Recall United States Terminated Historical recordClass II

First Source, LLC

Product
Dark Chocolate Almonds packaged under the brand names: (1)…
Reason
Chocolate products contain undeclared milk
Published
December 20, 2017
Distribution
AR, AZ, CA, CO, FL, GA, IL, KY, LA, MA,…

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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

View recall →

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

View recall →

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

View recall →

Data last updated:

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.