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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 13,141–13,160 of 20,397 recalls

FDA Recall Terminated Historical recordClass II

Phenylephrine HCL in 0.9% Sodium Chloride 10 mL, 1 mg/10 mL (100 mcg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-171-12

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Diltiazem HCl 125 mg in 5% Dextrose 125 mL Single-Dose- Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222; NDC 52533-103-13

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Norepinephrine Bitartrate 4 mg Added to 0.9% Sodium Chloride 250 mL (16 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-134-18

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Norepinephrine Bitartrate 16 mg Added to 0.9% Sodium Chloride 250 mL (64 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-288-18

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Norepinephrine Bitartrate 8 mg Added to 0.9% Sodium Chloride 250 mL (32 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-217-18

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Succinylcholine Chloride Injection Solution 5 mL, 100 mg/5 mL (20 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-067-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Succinylcholine Chloride Injection Solution 10 mL, 200 mg/10 mL (20 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-067-12

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Glycopyrrolate Injection Solution, 1 mL 0.2 mg/1 mL (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222; NDC 52533-028-45

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Glycopyrrolate Injection Solution, 2 mL 0.4 mg/2 mL (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222; NDC 52533-028-16

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Glycopyrrolate Injection Solution, 5 mL 1 mg/5 mL (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222; NDC 52533-028-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ephedrine Sulfate in 0.9% Sodium Chloride 5 mL, 50 mg/5 mL (10 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-118-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ephedrine Sulfate Injection Solution 1 mL, 50 mg/1 mL (50 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-258-45

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ephedrine Sulfate in 0.9% Sodium Chloride 5 mL, 25 mg/5 mL (5 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-019-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ephedrine Sulfate in 0.9% Sodium Chloride 10 mL, 50 mg/10 mL (5 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-019-12

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Nystatin Topical Powder, USP, 100,000 USP units per gram, 15 grams per bottle, Rx only, Vensun, NDC 42543-052-61

by X-Gen Pharmaceuticals Inc.

Reason
Presence of Foreign Substance: potential presence of plastic particles.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Garden Of Light Inc.

Product
WOODSTOCK ORGANIC MATCHA VANILLA OATS, 1.8 oz (50g) cup UPC…
Reason
Potential for Listeria contamination
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Coborn's, Inc

Product
Fudge Brownie, Net Wt. 9 oz. (0.6 lb.) (255g), with the foll…
Reason
Some Gluten Free Chocolate Chip Bars were incorrectly labeled as Gluten Free Fudge Brownies. The Gluten Free Chocolate Chip Bars that are incorrectly labeled as Gluten Free Fudge Brownies do contain milk.
Published
August 16, 2017
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass II

Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30

by PD-Rx Pharmaceuticals, Inc.

Reason
Failed Tablet/Capsule Specification: out of specification for tablet weight.
Published
August 9, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60

by Teva Pharmaceuticals USA

Reason
Failed Tablet/Capsule Specification; out of specification for tablet weight
Published
August 9, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets, USP 600 mg, 500-count bottle (Capsule Shaped), Rx only, Manufactured for: Time Cap Labs, Inc., 7 Michael Avenue Farmingdale, NJ 11735, USA, Manufactured by: Marksans Pharma Ltd. Plot No. L-82, L-83 Verna Indl. Estate, Verna, Goa-403 722, India, NDC 49483-603-50

by Time-Cap Laboratories, Inc.

Reason
Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles were found to contain some Ibuprofen Tablets USP 800 mg.
Published
August 9, 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.