FDA recall Z-1499-2021

ConMed Corporation · Class II · device

Product

KIT_INFINITY_BASE Custom Procedural Kit - Italy, containing Infinity ACL Tibial Elbow and Tip Guides product line, KTE100 and KTT100. For use in open and arthroscopic procedures for knee ligament reconstruction The procedural kits have no kit specific labeling. Each product within the kits has its own product specific labeling.

Reason for recall

Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system and could cause a delay in procedure and may require another device or alternate surgical method to be used

Distribution

International distribution in the countries of Canada, Italy.

Key facts

Status
Terminated
Initiation date
2021-03-26
Report date
2021-05-05
Termination date
2024-04-05
Voluntary/Mandated
Voluntary: Firm initiated
Location
Utica, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1499-2021