Zimmer Biomet, Inc.: Medical Device Recall in 2017 - (Recall #: Z-0160-2018)

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:

ROSA Surgical Device 2.5.8, a computer-controlled electromechanical arm to guide standard neurosurgical instruments.

Product Classification:

Class II

Date Initiated: November 6, 2014

Date Posted: November 29, 2017

Recall Number: Z-0160-2018

Event ID: 77626

Reason for Recall:

Potential failure of a force feedback sensor that may result in continued movement of an operating arm (rather than an immediate stop as intended).

Status: Terminated

Product Quantity: 31 units

Code Information:

Model No. 2.5.8., Serial No. RO10009, RO10011, RO10014, RO13023, RO13027, RO14031, RO14033, RO14035, and RO14037.

Distribution Pattern:

US distribution in AR, GA, OH, MI, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated