Z-1493-2018 Class II Ongoing

Recalled by Beijing Syntech Laser Co., Ltd — Beijing, N/A

Recall Details

Product Type
Devices
Report Date
May 9, 2018
Initiation Date
July 3, 2017
Termination Date
N/A
Voluntary/Mandated
FDA Mandated
Product Quantity
6

Product Description

Beijing Syntech Laser APOLLO JV+ Medical Platform surgical lasers

Reason for Recall

The noncompliance is that the certification label was not affixed on the product, with statement "Complies with 21 CFR 1040.10 and 1040.11 except for deviations pursuant to Laser Notice No. 50, dated June 24, 2007".

Distribution Pattern

US Distribution

Code Information

Model APOLLO 1V+Medical Platform