PlainRecalls
FDA Devices Moderate Class II Terminated

Conformis iTotal Cruciate Retaining (CR) Knee Replacement System- Orthopedic Implant Cat: TCR-121-1111-010102, (ITOTAL CR IPOLY XE IMPLANT KIT LEFT)

Reported: September 2, 2020 Initiated: July 20, 2020 #Z-2849-2020

Product Description

Conformis iTotal Cruciate Retaining (CR) Knee Replacement System- Orthopedic Implant Cat: TCR-121-1111-010102, (ITOTAL CR IPOLY XE IMPLANT KIT LEFT)

Reason for Recall

Outer box labels for kit 0469247 correct, however the boxes contained the implants and jigs for 0468920

Details

Recalling Firm
Conformis, Inc.
Units Affected
1 kit
Distribution
NV
Location
Billerica, MA

Frequently Asked Questions

What product was recalled?
Conformis iTotal Cruciate Retaining (CR) Knee Replacement System- Orthopedic Implant Cat: TCR-121-1111-010102, (ITOTAL CR IPOLY XE IMPLANT KIT LEFT). Recalled by Conformis, Inc.. Units affected: 1 kit.
Why was this product recalled?
Outer box labels for kit 0469247 correct, however the boxes contained the implants and jigs for 0468920
Which agency issued this recall?
This recall was issued by the FDA Devices on September 2, 2020. Severity: Moderate. Recall number: Z-2849-2020.