McKesson PREVENT HT Safety Winged Blood Collection Needles with specific lot numbers recalled due to potential safety mechanism activation issues. Affected units may have difficulty triggering the safety feature during use.
Potential for difficulty in safety mechanism activation.
McKesson PREVENT HT Safety Winged Blood Collection Needles with specific lot numbers are being recalled because they may have difficulty activating the safety mechanism. This could lead to injury during blood draws if the safety feature doesn't engage properly.
The safety mechanism in these needles may not activate correctly during use, which could result in injury if the needle is not properly secured. This is a potential risk during blood collection procedures.
Healthcare professionals and patients who use these needles for blood draws may be affected. Those with the specific lot numbers listed are most at risk.
Check the product label for the manufacturer's lot number and expiration date. Affected units have specific lot numbers: CKDI11-01 (exp. 2024-10-01), CKDI12-01 (exp. 2024-11-01), CKDJ01-01 (exp. 2024-12-01), CKDJ03-01 (exp. 2025-02-01), or CKDJ05-01 (exp. 2025-04-01).
Look for the lot number and expiration date on the needle packaging or label.
Reach out to McKesson PREVENT HT for further assistance or to confirm if your specific model is affected.
The recall is due to potential difficulty in activating the safety mechanism, which could lead to injury during blood collection.
Affected lot numbers include CKDI11-01 (exp. 2024-10-01), CKDI12-01 (exp. 2024-11-01), CKDJ01-01 (exp. 2024-12-01), CKDJ03-01 (exp. 2025-02-01), and CKDJ05-01 (exp. 2025-04-01).
No, but you should check the lot number and expiration date to see if your needles are affected. If they are, contact the manufacturer for guidance.
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-0206-2022 — McKesson PREVENT HT McKesson PREVENT HT Hello, I own a McKesson PREVENT HT that is covered by recall Z-0206-2022 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.
