Device recall: Beijing Syntech Laser Diode Laser surgical lasers
Class II FDA enforcement event 79697. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
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".
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Beijing Syntech Laser Co., Ltd started this device recall on 3 Jul 2017. The firm address in the FDA record is in Beijing. FDA put the recall in Class II. FDA event 79697 has 8 product records. The first FDA enforcement report date is 9 May 2018. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
US Distribution
Recalling firm
Beijing Syntech Laser Co., Ltd, Beijing, N/A, China.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: FDA Mandated.
Products
8 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1488-2018 | Beijing Syntech Laser Diode Laser surgical lasers | 13 | Class II | Ongoing | 9 May 2018 |
| Z-1489-2018 | Beijing Syntech Laser Trixel C02 Laser surgical lasers | 38 | Class II | Ongoing | 9 May 2018 |
| Z-1490-2018 | Beijing Syntech Laser Trixel 11 C02 Laser surgical lasers | 3 | Class II | Ongoing | 9 May 2018 |
| Z-1491-2018 | Beijing Syntech Laser UL C02 Laser surgical lasers | 92 | Class II | Ongoing | 9 May 2018 |
| Z-1492-2018 | Beijing Syntech Laser APOLLO V+ Medical Platform surgical lasers | 11 | Class II | Ongoing | 9 May 2018 |
| Z-1493-2018 | Beijing Syntech Laser APOLLO JV+ Medical Platform surgical lasers | 6 | Class II | Ongoing | 9 May 2018 |
| Z-1494-2018 | Beijing Syntech Laser Nice Station Light Based Platform surgical lasers | 7 | Class II | Ongoing | 9 May 2018 |
| Z-1495-2018 | Beijing Syntech Laser UL Station surgical lasers | 199 | Class II | Ongoing | 9 May 2018 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2017
- 1,091
- Share of these events in Class II
- 93%
- Product records in this event
- 8
- Events of the firm on the register
- 1
Official channels
- FDA enforcement report Z-1488-2018The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 79697. https://recallregister.com/fda/ii/79697/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
US Distribution
- What quantity of product is in FDA event 79697?
- The event has 8 product records. The first record gives this quantity:
13
- How did the recall start?
- The FDA record says:
FDA Mandated
- How many device recalls of 2017 have the same class?
- 93% of the 1,091 device events that started in 2017 are in Class II.