Delta Med recalls specific lots of DELTAVEN Safety IV Catheters with closed systems due to possible sterility issues. Affected units include REF 3836272, 3814272, 3845272, and 3856272 with corresponding lots. Consumers should check their catheters against the listed references.
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Delta Med is recalling specific lots of DELTAVEN Safety IV Catheters with closed systems because of possible sterility issues. This could lead to infections if the catheters are not properly sterilized. Affected units have unique reference numbers and lots listed in the recall notice.
The recall is for possible missing sterility in the medical devices. If the catheters are not properly sterilized, they could cause infections during medical procedures. This risk is related to the manufacturing process and not normal use.
Healthcare professionals and patients using the DELTAVEN Safety IV Catheters with closed systems in specific lots are affected. Those with the listed reference numbers and lots are most at risk.
Check your DELTAVEN Safety IV Catheter for reference numbers: 3836272, 3814272, 3845272, or 3856272. Also, verify the lot numbers: 11T80188, 11T80272, 12T80147, or 12T80347.
Look for reference numbers 3836272, 3814272, 3845272, or 3856272 and corresponding lot numbers.
The recall is due to possible missing sterility in the medical devices, which could lead to infections if not properly sterilized.
Check your catheter for the reference numbers and lot numbers listed in the recall notice. If you have them, contact Delta Med for further instructions.
The recall states possible sterility issues, which could lead to infections. However, the exact risk level is not specified in the notice.
We’ve drafted a message you can send Delta Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2295-2021 — Delta Med Delta Med Hello, I own a Delta Med that is covered by recall Z-2295-2021 from Delta Med. 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.
