Beijing Syntech Laser APOLLO JV+ Medical Platform surgical lasers

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Model APOLLO 1V+Medical Platform
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Beijing Syntech Laser Co., Ltd
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".
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Beijing Syntech Laser APOLLO JV+ Medical Platform surgical lasers

Product Codes/Lot Numbers:

Model APOLLO 1V+Medical Platform

Distribution:

Distributed in: US

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1493-2018

Related Recalls

Class I - Dangerous

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".

Jul 3, 2017 Surgical Instruments View Details →
Class I - Dangerous

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".

Jul 3, 2017 Surgical Instruments View Details →
Class I - Dangerous

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".

Jul 3, 2017 Surgical Instruments View Details →