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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 12,121–12,140 of 18,028 recalls

FDA Recall Terminated Historical recordClass I

Vancomycin HCl 750 mg added to 250 mL 0.9% Sodium Chloride For IV Use Only, Rx Only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0929-40

by SCA Pharmaceuticals

Reason
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Vancomycin HCl 1.5 gram added to 5% Dextrose 500 mL Total Approximate Volume 515 mL For IV Use Only, Rx Only , SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0925-44

by SCA Pharmaceuticals

Reason
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Vancomycin HCl 1.5 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use Only Rx Only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0924-59

by SCA Pharmaceuticals

Reason
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Vancomycin HCl 1.25 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use Only, Rx Only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0923-59

by SCA Pharmaceuticals

Reason
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Vancomycin HCl 1 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use Only, Rx Only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0920-59

by SCA Pharmaceuticals

Reason
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Vancomycin HCl 1.25 g added to 5% Dextrose 250 mL Bag For IV Use Only, Rx Only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0922-40

by SCA Pharmaceuticals

Reason
Presence of particulate matter - this recall is due to a recent Hospira recall of vancomyicn hydrochloride 10gm vials due to presence of particulate matter.
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Vancomycin Hydrochloride for Injection, USP, 10 grams, Pharmacy Bulk Package - Not For Direct Infusion, For Intravenous Use, packaged in 100 mL glass vial, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6510-01

by Hospira Inc., A Pfizer Company

Reason
Presence of Particulate Matter: A hair was found stuck to the stopper of inside a single vial. The hair came in contact with the reconstituted drug product.
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Ibuprofen Lysine Injection, 20 mg/2 mL (10 mg/mL), 2 mL Single-Dose Vial (NDC 39822-1030-1), packaged in 3 x 2 mL Single-Dose Vials per carton (NDC 39822-1030-2); Rx only, Distributed by: X-Gen Pharmaceuticals, Inc., Big Flats, NY 14814; Manufactured by: Exela Pharma Sciences, LLC, Lenoir, NC 28645.

by X-Gen Pharmaceuticals Inc.

Reason
Presence of Particulate Matter
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Ciclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15), b) 30 g tubes (NDC 0713-0638-31), and c) 90 g tubes (NDC 0713-0638-18), Rx only, Manufactured by: G&W Laboratories, Inc., South Plainfeld, NJ 07080.

by G & W Laboratories, Inc.

Reason
Labeling: Incorrect or Missing Package Insert: product lots packaged with an out-of-date insert.
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749601

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749501

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749401

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 50419-70305

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Nifedipine Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-370-01.

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Nifedipine Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-369-01.

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended Release Tablets, 60 mg, 100- count bottles, Rx only Manufactured for Almatica, Almatica Pharma Inc. Pinebrook, NJ 07058 USA, NDC 50419-702-05

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended Release Tablets 30 mg, 100-count bottles, Rx only, Manufactured for Bayer Healthcare Bayer Healthcare Pharmaceuticals Inc. Whippany, NJ 07901 Manufactured in Germany, NDC 50419-701-05

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Nifedipine Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-368-01.

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline, Research Triangle Park, NC 22709, NDC 0173-0682-20.

by GlaxoSmithKline, LLC

Reason
Defective Delivery System: Elevated number of units with out of specification results for leak rate.
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Kalbitor (ecallantide), 10mg/mL, packaged in 3 vials per Carton, Rx Only, Dynax Corp., Burlington, MA. NDC47783-101-01

by Shire

Reason
Presence of Particulate Matter: Glass
Published
April 12, 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.