FDA recall Z-1946-2020
Becton Dickinson & Company · Class II · device
Product
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Reason for recall
Iincorrectly packaged without the required lidocaine as labeled
Distribution
AZ, CT, GA, IL, LA, MA, MI, MN, ND, NE, NY, OH, SD, TX),
Key facts
- Status
- Terminated
- Initiation date
- 2020-03-17
- Report date
- 2020-05-20
- Termination date
- 2020-10-21
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Franklin Lakes, NJ, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1946-2020