Medline recalls convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN labeled RETINAL. The catheters may slow or fail to retract during insertion, potentially causing injury.
Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the Catheter, the needle is slow to retract or fails to retract.
Medline is recalling convenience kits that contain specific BD Insyte Autoguard Shielded IV Catheters. These catheters may slow or fail to retract during insertion, which could lead to injury if the needle does not move back properly.
During IV catheter insertion, the needle may slow to retract or fail to retract completely. This can cause the needle to remain in place longer than intended, increasing the risk of tissue damage or injury to the patient.
Healthcare professionals who use Medline convenience kits containing the specific BD Insyte Autoguard Shielded IV Catheters labeled RETINAL are most at risk. Patients receiving IV treatments with these catheters could experience injury if the needle does not retract properly.
Check for Medline convenience kits labeled 'RETINAL PACK-LF' with the reference number DYNJ0151148B. The kits may have a unique identifier (UDI/DI) 10889942050819 or 40889942050810.
Look for the label 'RETINAL PACK-LF' and reference number DYNJ0151148B on the kit.
If you have the recalled kit, stop using it immediately and contact Medline for instructions.
The catheters may slow to retract or fail to retract during insertion, which could cause injury.
Check for the label 'RETINAL PACK-LF' with reference number DYNJ0151148B and unique identifiers 10889942050819 or 40889942050810.
Stop using the kit immediately and contact Medline for instructions on how to return it.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2045-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2045-2025 from Medline. 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.
