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U.S. Department of Health and Human Services

Class 2 Device Recall McKesson PREVENT HT Safety Blood Collection Needle

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 Class 2 Device Recall McKesson PREVENT HT Safety Blood Collection Needlesee related information
Date Initiated by FirmAugust 24, 2021
Create DateNovember 05, 2021
Recall Status1 Terminated 3 on July 21, 2023
Recall NumberZ-0205-2022
Recall Event ID 88757
Product Classification Needle, hypodermic, single lumen - Product Code FMI
ProductMcKesson PREVENT HT Safety Blood Collection Needles, 22G 1 1/4 inch, MFR # 16-NBC22GS
Code Information Lot numbers / Expiration Date: CKDI11-01 / Exp. Date 2024-10-01, CKDI11-02 / Exp. Date 2024-10-02, CKDI12-01 / Exp. Date 2024-11-01, CKDJ01-01 / Exp. Date 2024-12-01, CKDJ03-01 / Exp. Date 2025-02-01, CKDJ05-01 / Exp. Date 2025-04-01, CKDJ05-03 / Exp. Date 2025-04-03, CKDJ06-01 / Exp. Date 2025-05-01, CKDJ12-01 / Exp. Date 2025-11-01.
FEI Number 3003560965
Recalling Firm/
Manufacturer		 Zhejiang Kindly Medical Devices Co., Ltd.
# 758 Binghai Five Rd.
Longwan Dist
Wenzhou China
For Additional Information Contact
8657708687200
Manufacturer Reason
for Recall		Potential for difficulty in safety mechanism activation.
FDA Determined
Cause 2		Nonconforming Material/Component
ActionOn 8/24/2021, Zhejiang Kindly Medical Devices Co., Ltd. issued Urgent Medical Device Safety Alert notices to two customers. On 9/17/2021, issued a second notice to customers dated 8/24/2021. Action to be Taken by User: 1 - Advise the user to lower the angle between safety protective cap and needle tube by slight pressing in the direction of activation, then using a thumb or hard surface to activate the safety protective cap and lock the needle tube in the IFU, then together with corresponding illustration. 2 - Request the user to strictly follow the guidance of the IFU.
DistributionU.S. Nationwide distribution.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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