Delta Med recalls specific DELTAVEN Y IV catheters due to potential sterility problems. Affected units include REF 3832072, 3810072, 3842072, and 3852072 with specific 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 certain DELTAVEN Y IV catheters that may not be sterile, which could lead to infections if used. This recall affects specific product references and lots sold in the U.S. The issue requires immediate attention to prevent health risks.
The catheters may not be properly sterilized, which could lead to infections if used. This risk occurs because the sterilization process might have failed, making the devices unsafe for medical procedures.
Healthcare professionals and patients using the recalled DELTAVEN Y IV catheters. Those with the specific product references and lots listed are most at risk.
Check the product reference (REF) numbers: 3832072, 3810072, 3842072, or 3852072. Also look for the specific lot numbers: 11T80190, 11T80303, 12T80342, or 12T80348.
Identify your DELTAVEN Y IV catheter's reference number and lot number to confirm if it's affected.
Reach out to Delta Med SpA directly for further instructions on how to handle the recalled items.
The recall is due to possible missing sterility in the medical devices, which could lead to infections if used.
The affected catheters have reference numbers 3832072, 3810072, 3842072, or 3852072 with specific lot numbers: 11T80190, 11T80303, 12T80342, or 12T80348.
Contact Delta Med SpA directly for instructions on how to handle the recalled items.
We’ve drafted a message you can send Delta Med to request your refund or repair — edit it as you like.
Subject: Recall Z-2298-2021 — Delta Med Delta Med Hello, I own a Delta Med that is covered by recall Z-2298-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
