FDA recall Z-2086-2019
Teleflex Medical · Class II · device
Product
Rusch EasyCath Kit
Reason for recall
Potential for product not to be sterile.
Distribution
Nationwide distribution to CA, FL, IL, NC, NJ, OH, OK, TX.
Key facts
- Status
- Terminated
- Initiation date
- 2019-07-01
- Report date
- 2019-08-07
- Termination date
- 2021-11-04
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Morrisville, NC, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2086-2019