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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 November 2026.

37,449
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 8,081–8,100 of 21,307 recalls

FDA Recall TerminatedTerminated: September 17, 2021Historical recordClass III

DELFELX Peritoneal Dialysis Solution with 4.25% Dextrose, Low Magnesium, Low Calcium, 5000 mL, Fresenius Medical Care, Waltham, MA 02451, NDC 49230-0212-50

by Fresenius Medical Care Holdings, Inc.

Reason
Temperature Abuse: Product exposed to temperature outside specified limits.
Published
June 16, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 17, 2021Historical recordClass III

DELFLEX Peritoneal Dialysis Solution with 2.5 % Dextrose, Low Magnesium, Low Calcium, packaged in a) 3000 mL 2 packs (NDC 49230-0209-23), b) 3000 mL (NDC 49230-209-30) and c) 5000 mL (NDC 49230-209-50) Rx only, Fresenius Medical Care NA Waltham, MA 02451

by Fresenius Medical Care Holdings, Inc.

Reason
Temperature Abuse: Product exposed to temperature outside specified limits.
Published
June 16, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 17, 2021Historical recordClass III

DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose, 5000 mL bags, 2-pack, Rx Only, Fresenius Medical Care NA, Waltham, MA 02451, NDC 49230-0188-50

by Fresenius Medical Care Holdings, Inc.

Reason
Temperature Abuse: Product exposed to temperature outside specified limits.
Published
June 16, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 17, 2021Historical recordClass II

Sodium Chloride 0.9%, USP, 1000 mL, Mfg by: Fresenius Medical Care North America, Waltham, MA 02451, NDC 46163-0300-10

by Fresenius Medical Care Holdings, Inc.

Reason
Temperature Abuse: Product exposed to temperature outside specified limits.
Published
June 16, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: August 6, 2021Historical recordClass I

RAINFIELD MARKETING GROUP

Product
Enoki Mushroom, 150g clear plastic bag with orange bottom; U…
Reason
California Department of Public Health sampled Enoki mushrooms at retail with a positive result for Listeria monocytogenes.
Published
June 16, 2021
Distribution
U.S. distribution to the following: CA,…

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FDA Recall United States TerminatedTerminated: February 9, 2022Historical recordClass I

Arizona Nutritional Supplements

Product
365 Everyday Value Whey Protein Powder Natural Vanilla Flavo…
Reason
Whey Protein Powder was mistakenly packaged with Soy Protein Powder.
Published
June 16, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: February 10, 2022Historical recordClass I

BCFoods, Inc.

Product
BC Foods Celery Stalk and Leaf Dice 3/8, AD Sulfites, 11 lb.…
Reason
Product contains ingredient which tested positive for Salmonella
Published
June 16, 2021
Distribution
Manufactures and distributors in WI, OH,…

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FDA Recall United States TerminatedTerminated: February 10, 2022Historical recordClass I

BCFoods, Inc.

Product
BC Foods AD Celery Stalk Canners, 25 lb. Poly lined bulk fib…
Reason
Product contains ingredient which tested positive for Salmonella
Published
June 16, 2021
Distribution
Manufactures and distributors in WI, OH,…

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FDA Recall TerminatedTerminated: April 4, 2023Historical recordClass I

1% Lidocaine HCl Injection, USP, 300 mg/30 mL (10 mg/mL), 30 mL Single-dose vial (NDC 0409-4279-16), packaged in 25 vials per tray (NDC 0409-4279-02), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA.

by PFIZER, INC

Reason
Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine Hydrochloride Injection, USP may contain 1% Lidocaine HCl Injection, USP and some vials labeled to contain 1% Lidocaine HCl Injection, USP may contain 0.5% Bupivacaine Hydrochloride Injection, USP
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 4, 2023Historical recordClass I

0.5% Bupivacaine Hydrochloride Injection, USP, 150 mg/30 mL (5 mg/mL), 30 mL Single-dose Teartop Vials (NDC 0409-1162-19), packaged in 25 vials per tray (NDC 0409-1162-02), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA.

by PFIZER, INC

Reason
Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine Hydrochloride Injection, USP may contain 1% Lidocaine HCl Injection, USP and some vials labeled to contain 1% Lidocaine HCl Injection, USP may contain 0.5% Bupivacaine Hydrochloride Injection, USP
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall CompletedHistorical recordClass II

BusPIRone Hydrochloride Tablets, USP, 15 mg, 100-count bottle, Rx only, Manufactured By: Oxford Pharmaceuticals, LLC Birmingham, Alabama 35211, NDC 69584-093-10

by Oxford Pharmaceuticals, LLC

Reason
Presence of Foreign Tablets/Capsules
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: October 18, 2022Historical recordClass III

Thiamine HCl Injection, USP 200 mg/2 mL (100mg/mL), 2 mL vials, packaged in 25 (2 mL multi-dose vial) per carton, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 USA; Manufactured by: Mylan Institutional, Galway, Ireland. NDC: 67457-196-02

by Mylan Institutional LLC

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date: Cartons with the correct lot number 200906 contain vials labeled with the incorrect lot number 200901.
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Genpak

Product
Bake n Show¿ Oven Ready Food Tray 16 ounce
Reason
The firm was notified via a customer complaint that they found foreign objects in the packaging of the product.
Published
June 9, 2021
Distribution
Product was shipped to the following sta…

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FDA Recall United States OngoingHistorical recordClass II

Genpak

Product
Bake n Show¿ Cake Tray Round & Bake n Show¿ Cake Tray Squa…
Reason
The firm was notified via a customer complaint that they found foreign objects in the packaging of the product.
Published
June 9, 2021
Distribution
Product was shipped to the following sta…

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FDA Recall United States OngoingHistorical recordClass II

Genpak

Product
Bake n Show¿ Pizza Cookie Tray 12"
Reason
The firm was notified via a customer complaint that they found foreign objects in the packaging of the product.
Published
June 9, 2021
Distribution
Product was shipped to the following sta…

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FDA Recall United States OngoingHistorical recordClass II

Genpak

Product
Bake n Show¿ Muffin Tray 4 Cavity Large, Bake n Show¿ Muff…
Reason
The firm was notified via a customer complaint that they found foreign objects in the packaging of the product.
Published
June 9, 2021
Distribution
Product was shipped to the following sta…

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FDA Recall United States OngoingHistorical recordClass II

Genpak

Product
Bake n Show¿ Angel Food Tray 8 Inch & 8 inch shallow
Reason
The firm was notified via a customer complaint that they found foreign objects in the packaging of the product.
Published
June 9, 2021
Distribution
Product was shipped to the following sta…

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FDA Recall United States OngoingHistorical recordClass II

Hi Tech Pharmaceuticals

Product
Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056…
Reason
The firm was notified by the FDA that the product contains the unapproved food additive 1,4-dimethylamylamine (DMAA).
Published
June 9, 2021
Distribution
The product was shipped to the following…

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FDA Recall United States TerminatedTerminated: July 5, 2021Historical recordClass II

Wegmans Food Markets, Inc.

Product
Wegmans Food You Feel Good About Everything Bagel Seasoned H…
Reason
Product may contain foreign object (pieces of hard black plastic).
Published
June 9, 2021
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio Yogurt Bar Mixed Berry Low Sugar Bar 50g x 10 Clio Reta…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
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.

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