Delta Med recalls two lots of IV catheters due to possible missing sterility. Affected units may not be safe for medical use. Contact for remedy details.
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Delta Med is recalling two specific lots of IV catheters because they might not be sterile. Using these catheters could lead to infections or other health risks if they are not properly sterilized.
The catheters may not be properly sterilized, which could lead to infections or other health issues if used in medical procedures. This risk occurs because the sterilization process might have failed for these specific lots.
Healthcare professionals and patients who use the recalled IV catheters are at risk. Those who have the specific lot numbers listed are most affected.
Check the product label for the lot numbers: REF 3738522 (Lot 00A2160813) or REF 373:822 (Lot 00A1160822). These are the only affected units.
Look for the lot numbers REF 3738522 (Lot 00A2160813) or REF 3738822 (Lot 00A1160822) on the catheter packaging.
The recall is due to possible missing sterility in the medical devices, which could lead to infections if used.
The official recall notice does not specify a remedy or action for affected units.
No, only the two specific lot numbers listed are affected.
We’ve drafted a message you can send Delta Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2303-2021 — Delta Med Delta Med Hello, I own a Delta Med that is covered by recall Z-2303-2021 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.
