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.

37,204
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,841
Class I recallsReasonable probability of serious health consequences
24,366
Class II recallsTemporary or medically reversible health consequences
2,892
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 2,073 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.

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)

  • 1,714 recalls have been announced year to date.
  • Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
  • Oct 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 II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 14,641–14,660 of 19,957 recalls

FDA Recall United States Terminated Historical recordClass II

Kabobs Inc

Product
MINI CLASSIC FRENCH QUICHE, 200 CT, Prepared by: Kabobs, 542…
Reason
Product was manufactured with flour recalled due to E. coli O121 contamination.
Published
October 26, 2016
Distribution
AR, CA, CO, CT, FL, GA, IL,IN, IO, KY, L…

View recall →

FDA Recall United States Terminated Historical recordClass II

Kabobs Inc

Product
MINI FLORENTINE QUICHE, 200 CT, Prepared by: Kabobs, 54234 N…
Reason
Product was manufactured with flour recalled due to E. coli O121 contamination.
Published
October 26, 2016
Distribution
AR, CA, CO, CT, FL, GA, IL,IN, IO, KY, L…

View recall →

FDA Recall United States Terminated Historical recordClass II

Kabobs Inc

Product
MAC & CHEESE POPPERS, 100 CT, Prepared by: Kabobs, 54234 Nor…
Reason
Product was manufactured with flour recalled due to E. coli O121 contamination.
Published
October 26, 2016
Distribution
AR, CA, CO, CT, FL, GA, IL,IN, IO, KY, L…

View recall →

FDA Recall United States Terminated Historical recordClass II

Kabobs Inc

Product
PANANG SHRIMP, 200 CT, Prepared by: Kabobs, 54234 North Lake…
Reason
Product was manufactured with flour recalled due to E. coli O121 contamination.
Published
October 26, 2016
Distribution
AR, CA, CO, CT, FL, GA, IL,IN, IO, KY, L…

View recall →

FDA Recall United States Terminated Historical recordClass II

Kabobs Inc

Product
COZY SHRIMP, 200 CT, Prepared by: Kabobs, 54234 North Lake D…
Reason
Product was manufactured with flour recalled due to E. coli O121 contamination.
Published
October 26, 2016
Distribution
AR, CA, CO, CT, FL, GA, IL,IN, IO, KY, L…

View recall →

FDA Recall United States Terminated Historical recordClass I

Awareness Corporation

Product
Awareness Boost Tea Dietary Supplement Passion Fruit N…
Reason
Boost Tea is being recalled for potential Salmonella contamination.
Published
October 26, 2016
Distribution
U.S. distribution to the following; CA,…

View recall →

FDA Recall Terminated Historical recordClass II

morphine Sulfate, 1 mg per mL (5 mg per 5 mL), in 0.9% Sodium Chloride, Preservative Free (Contains Sulfites), 5 mL Total Volume in a syringe, For IV use, Rx only, PharMEDium, Product code 2R3181.

by PharMEDium Services, LLC

Reason
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

methadone HCl, 1 mg per mL, in 0.9% Sodium Chloride, 1 mL Total Volume in a syringe, For IV Use Only, Rx only, PharMEDium, Product code 2T6120.

by PharMEDium Services, LLC

Reason
Stability Data Does Not Support Expiry:potential loss of potency in drugs packaged and stored in syringes.
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL Citrate, 5 mcg per mL (10 mcg per 2 mL) in 0.9% Sodium chloride, 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3339.

by PharMEDium Services, LLC

Reason
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL Citrate Injection, 50 mcg per mL (100 mcg per 2 mL), 2 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3303.

by PharMEDium Services, LLC

Reason
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate, 10 mg per mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3347.

by PharMEDium Services, LLC

Reason
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

atropine Sulfate Injection, 0.4 mg per mL, 1 mg per 2.5 mL, 2.5 mL Total Volume in a syringe, For IV use, Rx only, PharMEDium, Product code 2R3324.

by PharMEDium Services, LLC

Reason
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Amikacin Sulfate Injection, USP, 1 gm/4 mL (250 mg/mL) Rx Only, Manufactured in Hungary For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-9040-01 (individual pack), NDC 0703-9040-03 (shelf-pack carton of 10 vials).

by Teva Pharmaceuticals USA

Reason
CGMP Deviations
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

TAZORAC (tazarotene) Gel 0.05%, Rx only, packaged in 15 x 3.5 g professional sample containers, Manufactured by: Allergan Inc., Irvine, CA 92512. UPC: 300238335159.

by Allergan Sales, LLC

Reason
Failed Content Uniformity Specifications
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

TAZORAC (tazarotene) Gel 0.05%, Rx only, For Dermatologic Use Only, Not for Ophthalmic Use, packaged in a) 30 g tubes (NDC: 0023-8335-03, UPC: 300238335036) and b)100 g tubes,(NDC: 0023-8335-10, UPC: 300238335104), Manufactured by: Allergan Inc., Irvine, CA 92512.

by Allergan Sales, LLC

Reason
Failed Content Uniformity Specifications
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

ZENATANE (isotretinoin capsules USP) 20 mg, 30 capsules per prescription pack, Rx Only, Manufactured by: Cipla Limited, Kurkumbh Village Pune 4138012 India, Manufactured for: Dr. Reddy's Laboratories Limited Bachupally 500 090 India, NDC 55111-136-81

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Marcaine 0.5% (bupivacaine HCl) injection, USP, 250 mg/50 mL (5 mg/mL), 50 mL Multiple-Dose Vial, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1610-50.

by Hospira Inc., A Pfizer Company

Reason
Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial prevented stopper from forming a seal allowing water to ingress and dilute the product causing it to be less than the labeled potency.
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Marcaine 0.25% (bupivacaine HCl) injection, USP, 125 mg/50 mL (2.5 mg/mL), 50 mL Multiple-Dose Vial, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1587-50.

by Hospira Inc., A Pfizer Company

Reason
Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial prevented stopper from forming a seal allowing water to ingress and dilute the product causing it to be less than the labeled potency.
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

mitoXANTRONE Injection USP (concentrate), 20 mg/10 mL (2 mg/mL), 10 mL Multiple Dose Vial, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-4685-01.

by Teva Pharmaceuticals USA

Reason
Failed Impurities/Degradation Specifications: potential failure to meet the specification for Impurity D throughout shelf-life.
Published
October 19, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

5% Dextrose Injection USP, 100mL in a 150 mL PAB container, Rx only, B. Braun Medical Inc. Irvine, CA 92614-5895 USA, NDC 00264-1510-32

by B. Braun Medical Inc

Reason
Non-Sterility: fungal contamination due to leaking containers.
Published
October 19, 2016
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.