FDA recall Z-0860-2020
Vitreq Bv · Class II · device
Product
VitreQ 25G Blunt Needles with luer-lock connector-REF : CN25.D05 GTIN: 8719214221645
Reason for recall
Microscopic tears of the sterile pouch may compromise sterility
Distribution
Nationwide
Key facts
- Status
- Terminated
- Initiation date
- 2019-12-17
- Report date
- 2020-02-05
- Termination date
- 2020-12-09
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Vierpolders, N/A, Netherlands
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0860-2020