Zimmer Spine, Inc. Recalls

Overview of recall records associated with Zimmer Spine, Inc., including dates, categories and classifications where available.

3recall records

Mar 30, 2016latest record date

Mar 9, 2016earliest record date

Recall history in this database

Classification mix: Class II: 3.

Medical DeviceMar 30, 2016

Zimmer Spine Instinct Java System recall — FDA Z-1190-2016

Zimmer Biomet is initiating a Medical Device Correction Notice to provide updated cleaning and disinfecting instructions for use of the Instinct Java System (IFU reference: 046WAN0000T) and…

Class IIFDA: TerminatedZimmer Spine, Inc.

Medical DeviceMar 30, 2016

Zimmer Spine Universal Clamp System recall — FDA Z-1189-2016

Zimmer Biomet is initiating a Medical Device Correction Notice to provide updated cleaning and disinfecting instructions for use of the Instinct Java System (IFU reference: 046WAN0000T) and…

Class IIFDA: TerminatedZimmer Spine, Inc.

Medical DeviceMar 9, 2016

Zimmer Spine Virage OCT Spinal Fixation System recall — FDA Z-1019-2016

Zimmer Biomet Spine is initiating a Medical Device Correction regarding the Virage OCT Spinal Fixation System by providing additional guidance in the Virage OCT Surgical Technique Manual.

Class IIFDA: TerminatedZimmer Spine, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Zimmer Spine, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.