PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: July 24, 2019 Initiated: June 10, 2019 #Z-1960-2019

Product Description

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

Reason for Recall

Lack of an adequate sterilization validation.

Details

Recalling Firm
Zimmer Biomet, Inc.
Units Affected
92
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.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only), Item Number 595509. Recalled by Zimmer Biomet, Inc.. Units affected: 92.
Why was this product recalled?
Lack of an adequate sterilization validation.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 24, 2019. Severity: Moderate. Recall number: Z-1960-2019.