FDA recall Z-2064-2018
C.R. Bard, Inc. · Class II · device
Product
Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)
Reason for recall
Foley Catheter with Incorrect Retainer Cap Print
Distribution
FL, NY, MN and TX Canada, Japan and Taiwan
Key facts
- Status
- Terminated
- Initiation date
- 2017-12-13
- Report date
- 2018-06-13
- Termination date
- 2020-12-14
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Covington, GA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2064-2018