PlainRecalls
FDA Devices Moderate Class II Ongoing

Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: IV START BOX, REF ACC010665

Reported: July 9, 2025 Initiated: May 23, 2025 #Z-2044-2025

Product Description

Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: IV START BOX, REF ACC010665

Reason for Recall

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.

Details

Units Affected
36 units
Distribution
US Nationwide distribution in the states of IN, KY, CA, MI, TX, WA.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: IV START BOX, REF ACC010665. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 36 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 9, 2025. Severity: Moderate. Recall number: Z-2044-2025.