Recall Z-0209-2022— Zhejiang Kindly Medical Devices Co., Ltd.
Class II · Terminated
Class II FDA medical device recall by Zhejiang Kindly Medical Devices Co., Ltd., initiated 2021-08-24, terminated 2023-07-21. FDA's recall record names no specific 510(k) clearance for this event. Product: HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068, 100pcs/box 1000pcs/ctn 350*210*350mm. Reason: Potential for difficulty in safety mechanism activation..
- Recalling firm
- Zhejiang Kindly Medical Devices Co., Ltd.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-08-24
- Terminated
- 2023-07-21
- Firm location
- Wenzhou, N/A, China
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.