PlainRecalls
FDA Devices Moderate Class II Ongoing

MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013

Reported: February 8, 2023 Initiated: December 22, 2022 #Z-1047-2023

Product Description

MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013

Reason for Recall

The recall is due to observed intra-operative screw failure. When pre-drilled with ¿1.3mm drill bit for ¿2.0mm screws and ¿1.6mm drill bit for ¿2.4mm we have observed screw failure due to excessive torque.

Details

Units Affected
190 units
Distribution
US Nationwide distribution.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 190 units.
Why was this product recalled?
The recall is due to observed intra-operative screw failure. When pre-drilled with ¿1.3mm drill bit for ¿2.0mm screws and ¿1.6mm drill bit for ¿2.4mm we have observed screw failure due to excessive torque.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 8, 2023. Severity: Moderate. Recall number: Z-1047-2023.