FDA recall Z-1297-2018
Arrow International Inc · Class II · device
Product
Large Volume Abdominal Paracentesis Kit
Reason for recall
Product packaging may not be completely sealed.
Distribution
Nationally
Key facts
- Status
- Terminated
- Initiation date
- 2017-10-24
- Report date
- 2018-04-11
- Termination date
- 2020-04-17
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Reading, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1297-2018