Medline recalls specific IV kits containing BD Insyte Autoguard Shielded IV Catheters that may slow or fail to retract during insertion, risking injury. Affected kits have unique identifiers.
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 with certain IV catheters that may slow or fail to retract during insertion. This could lead to injury if the catheter doesn't move properly as it's inserted into a patient.
During IV catheter insertion, the needle may slow to retract or fail to retract, which could cause the catheter to become stuck or cause injury to the patient's vein or tissue.
Healthcare professionals using Medline convenience kits with BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN labeled 'IV START' are most at risk. Patients receiving IV treatments with these kits could also be affected.
Check for kits labeled 'IV START BOX' with reference number ACC010665. Look for unique identifiers: UDI/DI 10195327334918 (each) and 40195327334919 (case), Lot Number 24LDA590.
Look for the label 'IV START BOX' with reference number ACC010665 and unique identifiers UDI/DI 10195327334918 (each) and 40195327334919 (case).
The catheters may slow or fail to retract during insertion, which could cause injury to the patient's vein or tissue.
Check the kit label for the reference number ACC010665 and unique identifiers. If you have these identifiers, contact Medline for instructions.
The recall states the catheters may slow or fail to retract during insertion, which could lead to injury, but no specific injury severity is mentioned.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2044-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2044-2025 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.
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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.
