Encore Medical, Lp: Medical Device Recall in 2019 - (Recall #: Z-2090-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Flexible Drill Shaft, FMP Acetabular System Instrumentation REF 803-05-239 RX Encore Medical, L.P.

Product Classification:

Class II

Date Initiated: September 19, 2018

Date Posted: August 7, 2019

Recall Number: Z-2090-2019

Event ID: 83037

Reason for Recall:

Manufacturing error, the drill bit shaft is unable to properly capture the drill bit pin. Failure of the drill bit shaft to capture the drill bit pin could result in the drill bit coming loose which could result in a delay in surgery or adverse patient reaction resulting in a revision surgery.

Status: Ongoing

Product Quantity: 21

Code Information:

Lot # 262667L01

Distribution Pattern:

US ( MS, NY, MO, OK, UT, AZ)

Voluntary or Mandated:

Voluntary: Firm initiated