McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder (MFR #16-NBCH21GS) recalled due to potential safety mechanism activation issues. Affected units have specific lot numbers and expiration dates listed.
Potential for difficulty in safety mechanism activation.
McKesson PREVENT HT Safety Winged Blood Collection Needles with Tube Holder (MFR #16-NBCH21GS) are being recalled because the safety mechanism might not activate properly. This could lead to injury during blood draws if the needle is not safely secured.
The safety mechanism in the needle might not activate correctly, which could cause the needle to become unsafe during blood collection. This might lead to injury if the needle is not properly secured after use.
Healthcare professionals and patients who use the recalled needles for blood draws. Those who have the specific lot numbers and expiration dates listed are most at risk.
Check the product for the manufacturer's part number 16-NBCH21GS. The affected units have specific lot numbers: CKDI11-01 through CKDJ06-01 with corresponding expiration dates from October 2024 to May 2025.
Verify the manufacturer's part number and lot numbers to confirm if your needle is affected.
The safety mechanism might not activate properly, which could lead to injury during blood collection.
Check the product for the manufacturer's part number 16-NBCH21GS and lot numbers listed in the recall notice to see if it's affected.
Yes, the safety mechanism might not activate correctly, which could cause injury during blood draws.
We’ve drafted a message you can send McKesson PREVENT HT to request your refund or repair — edit it as you like.
Subject: Recall Z-0207-2022 — McKesson PREVENT HT McKesson PREVENT HT Hello, I own a McKesson PREVENT HT that is covered by recall Z-0207-2022 from McKesson PREVENT HT. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
