FDA recall Z-1960-2019

Zimmer Biomet, Inc. · Class II · device

Product

Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only), Item Number 595509

Reason for recall

Lack of an adequate sterilization validation.

Distribution

The products were distributed US nationwide. The products were distributed to the following foreign countries: Argentina, Australia, Canada, Chile, China, Columbia, Costa Rica, Ecuador, India, Japan, Korea, Malaysia, Mexico, Netherlands, Thailand, Venezuela.

Key facts

Status
Terminated
Initiation date
2019-06-10
Report date
2019-07-24
Termination date
2020-09-10
Voluntary/Mandated
Voluntary: Firm initiated
Location
Warsaw, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1960-2019