FDA recall record

Beijing Syntech Laser UL Station surgical lasers recall — FDA Z-1495-2018

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…

Class IIclassification
Z-1495-2018official record ID
May 9, 2018report date

Recall record at a glance

Official recordZ-1495-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBeijing Syntech Laser Co., Ltd
Report dateMay 9, 2018
Recall initiation dateJul 3, 2017
Quantity199
LocationBeijing, N/A, China

Official product description

Beijing Syntech Laser UL Station surgical lasers

Why the product was recalled

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 information

US Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: FDA Mandated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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