Delta Med recalls specific WOLF-PAK Self Safe Safety IV Catheters due to possible missing sterility. Affected models include REF PIVD2010W, PIV2210W, and PIV2475W with listed lots. Consumers should contact Delta Med for details.
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Delta Med is recalling three specific models of WOLF-PAK Self Safe Safety IV Catheters because they may not be sterile. This could lead to infections if used improperly. The recall affects patients receiving IV treatments who own these specific catheter models.
The catheters may not be sterile due to issues in the sterilization process. If used without proper sterility, they could cause infections in patients. This is a potential risk but not an immediate danger in normal use.
Patients receiving IV treatments who own the recalled catheter models (REF PIVD2010W, PIV2210W, or PIV2475W) are most at risk. Healthcare providers using these catheters for medical procedures may also be affected.
Check the product label for the model reference: PIVD2010W, PIV2210W, or PIV2475W. Also look for the lot numbers listed: 1100256, 1100316, or 1200084.
Look for the model reference (PIVD2010W, PIV2210W, or PIV2475W) and lot number on the catheter packaging.
The recall is due to possible missing sterility in the sterilization process, which could lead to infections if used improperly.
The affected models are REF PIVD2010W, REF PIV2210W, and REF PIV2475W with specific lot numbers.
The recall does not require immediate stop use; however, affected users should check with Delta Med for further instructions.
We’ve drafted a message you can send Delta Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2305-2021 — Delta Med Delta Med Hello, I own a Delta Med that is covered by recall Z-2305-2021 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.
