Public Health Trace

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.

37,115

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

State: AS ×
Clear all

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

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated September 16, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

BAC 225MCG/ BUP 4.5MG/ CLON 9MCG/ MORP 3MG/ML ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BAC 200MCG/BUP22MG/CLON210MCG/HYDROM 15MG/SUF800MCG/ML ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BAC 200MCG/ CLONI 250MCG/ MORP 10MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BAC 15MCG/HYDROM 15MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BAC 150 mcg/BUP 2 mg/Hydrom 15 mg/Morp 20 mg/SUF 650 mcg/mL Inj. in 20 mL syringe Assurance Infusion (713)533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Autologous Serum 20% Eye Drops in 3 mL droppers Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Alprostadil 40 mcg/mL (2 mL vial) Inj. Soln. in 2 mL vials Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ketorolac Tromethamine Injection, USP 60 mg/2 mL (30 mg/mL), packaged in 2 mL Single Dose Vials (NDC 0641-6043-01), 25 vials/shelf-pack (NDC 0641-6043-25), For IM Use Only, Rx only, Manufactured by: WEST-WARD Eatontown, NJ 07724 USA.

by Hikma Pharmaceuticals USA Inc.

Reason: Presence of Particulate Matter: particles identified as polydimethylsiloxane (PDMS)
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

TRIMIX FORTE 4 (UA) 30MG/3MG/30MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

TESTOSTERONE CYP 200MG/ML OIL in 10 mL vial Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

QUADMIX FORTE 30MG/4MG/40MCG/400MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

MORPHINE 1MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

LIPO B 25MG/50MG/50MG/1000MCG/ML (10ML VIAL) in 20 mL syringe and 10 mL vial Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

IPAMORELIN 2000MCG/ML INJ in 2 mL vial Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HYDROMORPHONE 2MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HYDROMORPHONE 1MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HYDROM 1MG/MORP 20MG/SUF 100MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HYDROM 17MG/PRIALT 5MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HCG 3000U/1ML INJ in 4 mL vial Assurance Infusion (713)533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

FENTANYL 1000MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

Data last updated: September 16, 2026 ET

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.