Delta Med recalls NEO DELTA SELFSAFE PUR 1 IV catheters (Lot 00A1160806) due to possible missing sterility. This could lead to infection risks if used improperly.
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Delta Med is recalling its NEO DELTA SELFSAFE PUR 1 IV catheters because they may not be sterile. Using these catheters could increase infection risk, especially in medical settings.
The catheters may not be properly sterilized, which could lead to infections if used in medical procedures. This is a potential issue for devices that come into contact with the body.
Healthcare professionals and patients using the recalled IV catheters. Those with the specific lot number (00A1160806) are most at risk.
Check for the lot number 00A1160806 on the catheter packaging. The product is the NEO DELTA SELFSAFE PUR 1 IV catheter from Delta Med SpA.
Look for the lot number 00A1160806 on the catheter packaging to confirm if it is recalled.
The recall indicates possible missing sterility, so it is not recommended for use until the recall is addressed.
Check the lot number on the packaging; if it is 00A1160806, contact Delta Med for instructions.
The recall record does not specify a replacement process or remedy.
We’ve drafted a message you can send Delta Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2302-2021 — Delta Med Delta Med Hello, I own a Delta Med that is covered by recall Z-2302-2021 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.
