PlainRecalls
FDA Devices Moderate Class II Ongoing

TEMA Axle Small, REF 1590.15.010 (additional information is pending receipt of the firm's product label/labeling)

Reported: March 22, 2023 Initiated: January 25, 2023 #Z-1261-2023

Product Description

TEMA Axle Small, REF 1590.15.010 (additional information is pending receipt of the firm's product label/labeling)

Reason for Recall

Due to the incorrect component, that is not cleared to be marketed in the U.S., being included in its elbow prosthesis.

Details

Recalling Firm
Limacorporate S.p.A
Units Affected
5 systems
Distribution
U.S. Distribution to: TX
Location
San Daniele Del Friuli, N/A

Frequently Asked Questions

What product was recalled?
TEMA Axle Small, REF 1590.15.010 (additional information is pending receipt of the firm's product label/labeling). Recalled by Limacorporate S.p.A. Units affected: 5 systems.
Why was this product recalled?
Due to the incorrect component, that is not cleared to be marketed in the U.S., being included in its elbow prosthesis.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 22, 2023. Severity: Moderate. Recall number: Z-1261-2023.