Smith & Nephew, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0548-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND

Product Classification:

Class II

Date Initiated: January 4, 2022

Date Posted: February 9, 2022

Recall Number: Z-0548-2022

Event ID: 89382

Reason for Recall:

The affected screwdrivers are out of specification and may not mate with the Surfix Alpha Lock screw

Status: Ongoing

Product Quantity: 8 units (US)

Code Information:

UDI: (01)10381780052234 (11)21101 (10)FVRG, Batch Numbers: FTL9, FTLA, and FVRG

Distribution Pattern:

US Nationwide distribution in the states of CA and OH.

Voluntary or Mandated:

Voluntary: Firm initiated