Skip to main content
Get Alerts

Data Explorer

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.

37,063
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 2,601–2,620 of 17,299 recalls

FDA Recall Terminated Historical recordClass II

Cefuroxime 4mg /0.4 mL (10 mg/mL), 1mL syringe, Rx only, Compounded by: Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.

by Pine Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Moxifloxacin in Balanced Salt Solution, Solution for Intraocular Injection, 600 mcg/0.4mL (150 mcg/0.1mL) Syringe, Rx only, Compounded by: Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.

by Pine Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Tropi-Phen (Tropicamide 1% phenylephrine HCl 2.5%) ophthalmic solution, 15 mL multi-use Droppers, Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.

by Pine Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Calcium Gluconate 2.5% solution for inhalation, 5mL pre-filled syringes, Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.

by Pine Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Calcium Gluconate Ophthalmic Irrigation Solution 1%, 500 mL bags, Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.

by Pine Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Endophth Kit (Vancomycin 1mg/0.1 mL - Ceftazidime 2.25mg/0.1 mL), Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.

by Pine Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Vancomycin 1 MG/0.1 ML Solution for Intraocular Injection, 0.8 ML Single Dose Vial, Rx only, Compounded by: Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.

by Pine Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Bevacizumab 1.25 MG/0.05 ML Solution for Injection, 1 mL syringes, Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.

by Pine Pharmaceuticals, LLC

Reason
Lack of Assurance of Sterility
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Betaxolol Tablets, USP 10 mg, Rx Only, 100 count bottles, Mfd by: KVK Tech Inc., Newtown, PA 18940, Made in USA, NDC# 10702-013-01.

by KVK-Tech, Inc.

Reason
Presence of Foreign Tablets/Capsules: There is a potential presence of oxycodone HCl tablets, USP 5 mg in bottles.
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Doxil (doxorubicin hydrochloride liposome injection) 50 mg in 25 mL (2 mg/mL), Single-Dose Vial, Rx only, Manufactured for: Baxter Healthcare Corporation, Deerfield, IL 60015. NDC 0338-0067-01

by Baxter Healthcare Corporation

Reason
CGMP Deviations: Product was exposed to temperatures exceeding the labeled storage conditions during transportation were released by mistake.
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Sucralfate Oral Suspension, 1g per 10mL, 16 oz (414 mL) PET bottle (12 bottles per case), Rx Only, Manufactured and Distributed by: VistaPharm, Inc. Largo, FL 33771 USA, NDC 66689-305-16

by VistaPharm LLC

Reason
Microbial Contamination of Non-Sterile Products: identified as Bacillus cereus.
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass I

TheraBreath for Kids! Oral Rinse, sodium fluoride 0.05% (0.02% w/v fluoride ion), 16 fl. oz. 473 mL bottles, Strawberry Splash, UPC 6 97029 70000 6, manufactured for Church & Dwight Co, Inc., Ewing, NJ 08628

by Church & Dwight Inc

Reason
Microbial contamination of Non-Sterile Product; presence of yeast identified as Candida parapsilosis
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail stores.

by Dollar Tree Distribution, Inc.

Reason
CGMP Deviations: OTC products were stored outside of labeled temperature requirements.
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Bupropion Hydrochloride Extended-Release Tablets USP (SR), 150 mg, 60 tablets bottle, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Limited Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 47335-737-86

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Dissolution Specifications
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

MYDRIATIC-4: Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile Ophthalmic Solution Drops 1% - 0.5% - 2.5% - 0.5%, 5mL bottle, Imprimis, NJOF, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852 (844)-446-6979, NDC:71384-632-05

by Imprimis NJOF, LLC

Reason
Subpotent: Out of Specification result observed for Ketorolac assay levels, below the 90.0-110.0% of label claim.
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall United States Completed Historical recordClass II

HEINZ

Product
Kraft Singles American Pasteurized Prepared Cheese product,…
Reason
Plastic fragment. Product is recalled due to potential for a thin strip of the primary packaging film to remain adhered to the cheese slice after the wrapper has been removed.
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Completed Historical recordClass I

BREXAFEMME (Ibrexafungerp) tablets 150 mg, 4 count cartons, Rx Only, Manufactured for and distributed by SCYNEXIS, Inc., Jersey City, NJ 07302 NDC 75788-115-04

by Scynexis, Inc.

Reason
Cross Contamination with Other Products: Potential cross-contamination of ibrexafungerp citrate drug substance with ezetimibe (a non-antibacterial beta-lactam compound).
Published
October 18, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Triamcinolone Acetonide Injectable Suspension, USP, 400 mg per 10 mL (40mg/mL), 10 mL Multiple Dose Vial, Rx Only, For Intramuscular or Intra-articular use only, Shake Well, Not for IV/ID, intraocular, epidural, or intrathecal use, Mfd. in India for Auromedics Pharma LLC., E Windsor, NJ, 08520, NDC 55150-385-01.

by Eugia US LLC

Reason
Presence of Particulate Matter: A product complaint of a piece of glass was identified in a vial. The piece of glass appears to be roughly 1 cm x 0.5 cm inside the vial.
Published
October 11, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use Intraocular injection Preservative Free NDC 71384-640-01 Not for resale. Office use only. Lot: 23APR018 Date Compounded: 24APR2023 Expires on: 17APR2024. In case of adverse event contact: www.fda.gov/medwatch or (800)-FDA-1088 Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B, Ledgewood, NJ, 07852 (844) 446-6979

by Imprimis NJOF, LLC

Reason
Subpotent: Failing Test Results for Epinephrine
Published
October 11, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC#: 68084-447-01; Individual Dose NDC: 68084-447-11

by Amerisource Health Services LLC

Reason
Failed Impurities/Degradation Specifications: Out of Specification results in the repackaged product for impurities at the 12-month time point.
Published
October 11, 2023
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.