Recall of 22G 1 1/4 inch blood collection needles with potential safety mechanism activation issues. Affected units include specific lot numbers and expiration dates.
Potential for difficulty in safety mechanism activation.
McKesson PREVENT HT Safety Blood Collection Needles (22G 1 1/4 inch) are being recalled due to potential difficulty in activating the safety mechanism. This could lead to improper needle use during blood draws.
The safety mechanism may not activate properly during use, potentially leading to improper needle disposal or injury. This could happen if the needle is not safely engaged after blood collection.
Healthcare professionals and individuals using these needles for blood collection may be affected. Those who have the specific lot numbers and expiration dates listed are most at risk.
Check for the manufacturer lot numbers: CKDI11-01 through CKDJ12-01 with expiration dates from October 2024 to November 2025. These needles are sold by McKesson PREVENT HT.
Look for the lot number on the needle packaging or label, which should match the listed numbers: CKDI11-01 through CKDJ12-01.
Reach out to McKesson PREVENT HT for further assistance if you have the affected needles.
The recall indicates a potential difficulty in safety mechanism activation, so they should not be used until the issue is resolved.
The expiration dates range from October 2024 to November 2025, depending on the lot number.
The recall does not specify a replacement process; contact McKesson PREVENT HT directly for assistance.
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-0205-2022 — McKesson PREVENT HT McKesson PREVENT HT Hello, I own a McKesson PREVENT HT that is covered by recall Z-0205-2022 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.
