Gk Photonics recalls

Gk Photonics has 6 recalls on record with the FDA and USDA, the earliest in 2019 and the latest reported on 14 Aug 2019. 6 are still ongoing.

Total recalls6since 2019

Last 12 months0reported

Class I00% of total

Ongoing6latest 14 Aug 2019

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 6 100%Class III 0 0%

Why gk photonics is recalled

Other Reasons6100%

Product types

Other Medical Devices6100%

By year

20196100%

Ongoing gk photonics recalls

6 active

Reported	Class	Recall	Company	Reason	Where
14 Aug 2019Device	CLASS II	Spectrum Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA
14 Aug 2019Device	CLASS II	ClubMax Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA
14 Aug 2019Device	CLASS II	Atom Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA
14 Aug 2019Device	CLASS II	Maxim Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA
14 Aug 2019Device	CLASS II	Logolas Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA
14 Aug 2019Device	CLASS II	Burstberry Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA

All gk photonics recalls, newest first

6 total

Reported	Class	Recall	Company	Reason	Where
14 Aug 2019Device	CLASS II	Spectrum Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA
14 Aug 2019Device	CLASS II	ClubMax Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA
14 Aug 2019Device	CLASS II	Atom Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA
14 Aug 2019Device	CLASS II	Maxim Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA
14 Aug 2019Device	CLASS II	Logolas Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA
14 Aug 2019Device	CLASS II	Burstberry Laser Projection Series recalled by Gk Photonics	Gk Photonics	Other	CA

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.