Smith & Nephew, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1843-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM Product Number: 72204042 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone

Product Classification:

Class II

Date Initiated: March 15, 2017

Date Posted: April 26, 2017

Recall Number: Z-1843-2017

Event ID: 76824

Reason for Recall:

Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming

Status: Terminated

Product Quantity: N/A

Code Information:

Batch Numbers: F92143, F92147, G10380, G10382, G11216, G11217 G11231, G11232, G15940, G15943, G18835, G18836, G30219 G30220, G30254, G30255, G32180, G32182, G32183, G32184

Distribution Pattern:

Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE

Voluntary or Mandated:

Voluntary: Firm initiated