Delta Med recalls specific DELTAVEN Y DNL Safety IV catheters due to possible missing sterility. Affected units have unique reference and lot numbers. Consumers should check their catheters against the list.
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Delta Med is recalling certain DELTAVEN Y DNL Safety IV catheters because they may not be sterile. This could lead to infections if used. The recall includes specific reference and lot numbers.
The catheters may not be sterile due to issues with the sterilization process. If not properly sterilized, they could cause infections when used in medical procedures.
Patients using the recalled catheters for medical treatments are affected. Healthcare providers who have these specific units in their inventory are at risk.
Check the reference number (REF) and lot number on the catheter packaging. The affected units include specific REF numbers like 3832572, 3842572, and 3821572 with corresponding lot numbers.
Look for the reference number (REF) and lot number on the catheter packaging to determine if it is affected.
The recall is due to possible missing sterility in the catheters, which could lead to infections if used.
The affected models include REF 3832572, 3842572, 3821572, 3833572, 3831572, 3810572, and 3852572 with specific lot numbers.
Check the reference number (REF) and lot number on the catheter packaging against the list provided in the recall 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-2296-2021 — Delta Med Delta Med Hello, I own a Delta Med that is covered by recall Z-2296-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
