Oscor Inc. recalls Destino Twist 14F (also branded as Guidestar 14F)

Recalled February 23, 2022 · FDA recall Z-0646-2022 · Oscor

Hazard

There is potential for separation between the threaded hub and threaded cap at the proximal end of the device. · FDA Class II

Units

549 units

Sold at

Distribution to TN and PA in USA OUS distribution to Czech Republic

Description

There is potential for separation between the threaded hub and threaded cap at the proximal end of the device.

Product

Destino Twist 14F (also branded as Guidestar 14F)

Manufacturer(s)

Oscor Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →