Delta Med recalls specific DELTAVEN FASTFLASH safety IV catheters due to potential sterility problems. Affected units have unique reference and lot numbers. Consumers should check their product details to determine if they are impacted.
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Delta Med is recalling certain DELTAVEN FASTFLASH safety IV catheters because they may not be properly sterilized, which could lead to infections. This recall affects specific reference and lot numbers listed in the official notice.
The recall is due to potential missing sterility in the medical devices, which could result in infections if the catheters are used without proper sterilization. This issue arises from problems during the sterilization process of the catheters.
Patients and healthcare providers using the recalled DELTAVEN FASTFLASH IV catheters are at risk of infection if the device is not sterile. The most vulnerable are those who have recently used the affected units.
Check the reference (REF) number and lot number on the catheter packaging. Affected units include specific REF numbers like 3814773, 3835773, and others with corresponding lot numbers such as 11T00118.
Identify the reference (REF) number and lot number on the catheter packaging to determine if it is affected.
Delta Med is recalling specific DELTAVEN FASTFLASH safety IV catheters due to potential missing sterility, which could lead to infections if used without proper sterilization.
Check the reference (REF) number and lot number on the packaging. Affected units include specific REF numbers like 3814773 with lot numbers such as 11T00118.
The recall record does not specify a remedy, so contact Delta Med directly for guidance on next steps.
We’ve drafted a message you can send Delta Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2297-2021 — Delta Med Delta Med Hello, I own a Delta Med that is covered by recall Z-2297-2021 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.
