Magnolia Medical recalls Steripath Gen2 Blood Collection Systems (21G/23G) due to premature needle retraction complaints. Affected units have specific model numbers and lot numbers listed in the recall notice.
Due to an uptick of complaints associated with premature needle retraction of blood collection system.
Magnolia Medical is recalling its Steripath Gen2 Blood Collection Systems because users have reported premature needle retraction. This could lead to inaccurate blood tests or injury during blood draws if the needle retracts too soon.
The blood collection system may retract the needle too early during blood draws, potentially causing inaccurate test results or minor injury. This issue has been reported in complaints but does not typically cause serious harm.
Healthcare professionals and patients who use the Steripath Gen2 Blood Collection Systems for blood draws are likely affected. Those with the specific model numbers and lot numbers listed in the recall are at the highest risk.
Check for model numbers 2700-21-EN, 2700-23-EN, 27BD-21-EN, or 27BD-23-EN on the product. Affected units also have specific lot numbers listed in the recall notice.
Look for model numbers 2700-21-EN, 2700-23-EN, 27BD-21-EN, or 27BD-23-EN on the product.
Reach out to Magnolia Medical for further assistance if you have the affected model numbers.
Users have reported premature needle retraction, which can cause inaccurate blood tests or minor injury during blood draws.
Affected models include 2700-21-EN, 2700-23-EN, 27BD-21-EN, and 27BD-23-EN with specific lot numbers listed in the recall.
No, the recall indicates a low risk issue that does not typically cause serious injury, so you can continue using it but should check for the affected model numbers.
We’ve drafted a message you can send Magnolia Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0318-2022 — Magnolia Medical Magnolia Medical Hello, I own a Magnolia Medical that is covered by recall Z-0318-2022 from Magnolia Medical. 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.
