PlainRecalls
FDA Devices Moderate Class II Terminated

Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010

Reported: February 19, 2020 Initiated: October 2, 2019 #Z-1156-2020

Product Description

Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010

Reason for Recall

Inner draw rod, which threads into the cage may potentially be separated from the proximal knob of the inserter

Details

Recalling Firm
Medicrea International
Units Affected
14 units
Distribution
OH, VA
Location
Rillieux La Pape

Frequently Asked Questions

What product was recalled?
Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010. Recalled by Medicrea International. Units affected: 14 units.
Why was this product recalled?
Inner draw rod, which threads into the cage may potentially be separated from the proximal knob of the inserter
Which agency issued this recall?
This recall was issued by the FDA Devices on February 19, 2020. Severity: Moderate. Recall number: Z-1156-2020.