FDA recall Z-0209-2022
Zhejiang Kindly Medical Devices Co., Ltd. · Class II · device
Product
HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068, 100pcs/box 1000pcs/ctn 350*210*350mm
Reason for recall
Potential for difficulty in safety mechanism activation.
Distribution
U.S. Nationwide distribution.
Key facts
- Status
- Terminated
- Initiation date
- 2021-08-24
- Report date
- 2021-11-17
- Termination date
- 2023-07-21
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Wenzhou, N/A, China
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0209-2022