Delta Med recalls specific batches of NEO DELTA Self Safe T IV catheters due to potential sterility problems. Affected units may not be sterile, risking infection during medical procedures.
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Delta Med is recalling certain batches of NEO DELTA Self Safe T IV catheters because they may not be sterile. This could lead to infections if used in medical procedures.
The catheters may not have been properly sterilized during manufacturing, which could lead to contamination. If used without proper sterility, they might cause infections during medical procedures.
Healthcare professionals and patients using the recalled catheters for medical procedures. Those with the specific batch numbers listed are most at risk.
Check the product for batch numbers: REF 3779422 (Lot 00A1160635), REF 3769522 (Lot 00A1160656), or REF 3708522 (Lot 00A1160638).
Identify the batch number on the catheter packaging to see if it matches the recalled units.
The recall is due to possible missing sterility in the medical device, which could lead to infection risks during medical procedures.
The official notice does not specify a remedy, so contact Delta Med directly for guidance.
Yes, check for batch numbers: REF 3779422 (Lot 00A1160635), REF 3769522 (Lot 00A1160656), or REF 3708522 (Lot 00A1160638).
We’ve drafted a message you can send Delta Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2301-2021 — Delta Med Delta Med Hello, I own a Delta Med that is covered by recall Z-2301-2021 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.