FDA recall Z-1289-2024

Baxter Healthcare Corporation · Class II · device

Product

STERIS Boot Assembly, Traction Device, OT 1000, Part Number REF 10009192

Reason for recall

Three lots of the Boot Assembly, Traction Device are being recalled due to due to a customer report of an incorrectly oriented locking pin which caused the boot to detach from the traction system. If an impacted device is used during surgery, the boot may detach from the traction system, potentially leading to patient harm and a delay in surgery.

Distribution

US Nationwide distribution in the state of Alabama.

Key facts

Status
Ongoing
Initiation date
2024-02-14
Report date
2024-03-20
Voluntary/Mandated
Voluntary: Firm initiated
Location
Deerfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1289-2024