AGILENT TECHNOLOGIES INC./US recalls Agilent Resolution ctDx FIRST Sample Collection Kit, 500032
- Recall date
- February 17, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1358-2023
- FDA classification
- Class III
- Brand / firm
- AGILENT TECHNOLOGIES INC./US
- Sold / distributed
- U.S. Nationwide distribution in the states of CA, GA, IN, NJ, and TX. O.U.S.: None
Why it was recalled
Distributed sample collection kit with an unapproved instruction for use.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Agilent Resolution ctDx FIRST Sample Collection Kit, 500032
Get recall alerts
Free email alert whenever AGILENT TECHNOLOGIES INC./US has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: AGILENT TECHNOLOGIES INC./US