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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.

37,143
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 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

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 12,281–12,300 of 21,597 recalls

FDA Recall Terminated Historical recordClass II

Harmon Face Values, Saline Nasal Spray (sodium chloride), 0.65%, packaged as a) 1.5 FL OZ (44 mL) bottle UPC 7 27510 00501 0; b) 3 FL OZ (88 mL) bottle UPC 7 27510 00502 7, Distributed by Harmon Stores, Inc., Union, NJ 07083 USA.

by Product Quest Manufacturing LLC

Reason
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Published
October 24, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

FAMILY wellness, Sterile Saline, Nasal Mist, Saline Nasal Relief (0.9% Sodium Chloride Solution), 4.25 FL OZ (126 mL) can, Distributed by: Midwood Brands, LLC, 10611 Monroe Rd., Matthews, NC 28105, UPC 0 32251 11617 9.

by Product Quest Manufacturing LLC

Reason
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Published
October 24, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

DG health, No Drip, Nasal Pump Mist (oxymetazoline hydrochloride), 0.05%, 1 FL OZ (30 mL) bottle, Distributed by: Dolgencorp, LLC, 100 Mission Ridge, Goodlettsville, TN 37072, UPC 7 27510 00373 3 .

by Product Quest Manufacturing LLC

Reason
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Published
October 24, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Discount Drug Mart, Food Fair, Saline Nasal Spray (sodium chloride) 0.65%, packaged as a) 3 FL OZ (89 mL) bottle UPC 0 93351 01833 6; b) 1.5 FL OZ (45 mL) bottle UPC 0 93351 01834 3, Distributed by: Discount Drug Mart, 211 Commerce Drive, Medina, OH 44256

by Product Quest Manufacturing LLC

Reason
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Published
October 24, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

CVS Health, Saline Nasal Gel with Soothing Aloe, packaged as a) Baby Net Wt. 0.5 OZ (14.2 g) tube UPC 0 50428 58392 0 Product #282476; and b) Net Wt. 0.5 OZ tube (14.2 g) UPC 0 50428 31746 4 Product #896071; Distributed by CVS Pharmacy, Inc,. One CVS Drive, Woonsocket, RI 02895.

by Product Quest Manufacturing LLC

Reason
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Published
October 24, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

CVS Health, Baby Nasal Spray/Drops, Non-Medicated, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 29380 5 Product #459367.

by Product Quest Manufacturing LLC

Reason
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Published
October 24, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

CVS Health, Sterile Saline Nasal Mist (sodium chloride) Allergy & Sinus Relief, 3.0%, 4.25 OZ (126 g) can, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 41854 3.

by Product Quest Manufacturing LLC

Reason
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Published
October 24, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

CVS Health, Saline Nasal Spray, Nasal Moisturizing Spray, Contains: Sodium Chloride 0.65%, Benzyl Alcohol & Benzalkonium Chloride as Preservatives, 1.5 FL OZ (44 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 40814 8 Product #891465.

by Product Quest Manufacturing LLC

Reason
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Published
October 24, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

CVS Health, Sterile Saline Nasal Mist (sodium chloride) Saline Nasal Moisturizer, 0.9%, packaged in a) Net Wt. 1.52 OZ (43 g) can UPC 0 50428 37079 7 Product #896831; b) Net Wt. 4.25 OZ (120 g) can UPC 0 50428 36124 5; c) Children's Net Wt. 2 OZ (57 g) can UPC 0 50428 58685 3 Product #282472, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895.

by Product Quest Manufacturing LLC

Reason
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Published
October 24, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

DERMATONE (titanium oxide 6% and zinc oxide 4.7%) No-Touch Sunscreen Stick, SPF 50, Net Wt. 0.49 oz. (13.9g) stick, Distributed by: Beaumont Products, Inc. Kennesaw, GA 30144, UPC 0 20908 05100 3.

by Product Quest Manufacturing LLC

Reason
Microbial Contamination of Non-Sterile Products: sample tested positive for Staphylococcus aureus.
Published
October 24, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Thyroid, USP (Full Strength) Levothyroxine 112.1 mcg/grain Liothyronine 29.2 mcg/grain Active Pharmaceutical Ingredient Rx Only 1000 grams NDC 0395-6580-43 Packaged by: Humco Texarkana, TX 75501 USA

by Humco Holding Group, Inc

Reason
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Published
October 24, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Thyroid, USP (Porcine) Levothyroxine 36.3 mcg/grain Liothyronine 9.7 mcg/grain Active Pharmaceutical Ingredient Rx Only 100 grams NDC 0395-8077-62 Packaged by: Humco Texarkana, TX 75501 USA

by Humco Holding Group, Inc

Reason
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Published
October 24, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Thyroid, USP (Porcine) Levothyroxine 36.3 mcg/grain Liothyronine 9.7 mcg/grain Active Pharmaceutical Ingredient Rx Only 1000 grams NDC 0395-8077-43 Packaged by: Humco Texarkana, TX 75501

by Humco Holding Group, Inc

Reason
CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Published
October 24, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Tarry Medical Products, Inc.

Product
Product comes in a plastic bag which is labeled as follows:…
Reason
Microorganism found inside vial.
Published
October 24, 2018
Distribution
Direct to PA, WI, OH, GA, NE, CA

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FDA Recall United States Terminated Historical recordClass III

Quest Nutrition, LLC

Product
Quest Protein Bar Vanilla Almond Crunch Single Bar UPC# -…
Reason
Undeclared allergen; tree nut (almonds)
Published
October 24, 2018
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States Ongoing Historical recordClass II

COCA COLA BOTTLING COMPAN

Product
Sprite 12 FL OZ (355 mL) CONTAINS PHENYLALANINE CAFFEINE FRE…
Reason
Product contains plastic material.
Published
October 24, 2018
Distribution
Product was shipped to IL, IN, KY, MI, O…

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FDA Recall United States Ongoing Historical recordClass II

COCA COLA BOTTLING COMPAN

Product
NO SUGAR NO CALORIES Diet Coke 12 FL OZ (355 mL) CONTAINS PH…
Reason
Product contains plastic material.
Published
October 24, 2018
Distribution
Product was shipped to IL, IN, KY, MI, O…

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FDA Recall United States Ongoing Historical recordClass II

COCA COLA BOTTLING COMPAN

Product
CAFFEINE FREE Diet Coke 12 FL OZ (355 ml) CONTAINS PHENYLALA…
Reason
Product contains plastic material.
Published
October 24, 2018
Distribution
Product was shipped to IL, IN, KY, MI, O…

View recall →

FDA Recall Terminated Historical recordClass II

Prevacid 24HR (Lansoprazole) delayed-release capsules, 15 mg, 14 capsules per bottle in a carton containing 1 bottle (NDC: 0067-6286-14), 2 bottles (NDC: 0067-6286-28) or 3 bottles (NDC: 0067-6286-42), Over-the-counter, Distributed By: GSK Consumer Healthcare, Warren, NJ 07059.

by GLAXOSMITHKLINE NEBRASKA

Reason
CGMP deviations
Published
October 17, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Actoplus met XR (pioglitazone and metformin HCl, extended-release) tablets, 15 mg/1000 mg, Rx Only, 30 tablet bottle, Distributed by: Takeda Pharmaceuticals America, Inc, Deerfield, IL 60015. NDC: 64764-510-30

by Takeda Development Center Americas, Inc.

Reason
Defective Delivery System: tablets may be missing, in whole or in part, the laser drilled holes on the metformin core of the Actoplus met XR tablets.
Published
October 17, 2018
Distribution
AR, LA, MS, NC, NJ, OH, PA, SC and Puert…

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.