FDA Enforcement
Class II
Terminated
BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: Groshong Midline Bard MYPICC Kit 4F (Single-Lumen) The syringe is used to pre-flush the catheter prior to placement and may also be used to verify patency post-placement.
Recall: Z-1275-2015
·
Reported March 25, 2015
Enforcement
- Recall Number
- Z-1275-2015
- Event ID
- 70430
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Bard Access Systems
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- March 25, 2015
- Initiation Date
- August 8, 2014
- Classification Date
- March 13, 2015
- Termination Date
- August 5, 2015
- Address
- 605 N 5600 W, Salt Lake City, UT, 84116-3738, United States
Description
BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: Groshong Midline Bard MYPICC Kit 4F (Single-Lumen) The syringe is used to pre-flush the catheter prior to placement and may also be used to verify patency post-placement.
Reason
Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit open seals, which could impact product sterility. Bard includes these pouched syringes, attached to some configurations of PICC kits, Port Access kits (PAK), PowerGlide kits, Midline kits, and Convenience kits.
Code Info
Lot Numbers: 13FB8860 Product codes: CK000069
Distribution
US Nationwide Distribution.
Quantity
48 units