Oculus Optikgeraete recalls

Oculus Optikgeraete has 7 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 6 Sep 2023. 6 are still ongoing. The most frequent reason is device malfunction.

Total recalls7since 2018

Last 12 months0reported

Class I00% of total

Ongoing6latest 6 Sep 2023

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 7 100%Class III 0 0%

Why oculus optikgeraete is recalled

Device Malfunction457%
Lead & Heavy Metals343%

Product types

Other Medical Devices686%
Imaging Equipment114%

By year

2023343%
2022343%
2018114%

Ongoing oculus optikgeraete recalls

6 active

Reported	Class	Recall	Company	Reason	Where
6 Sep 2023Device	CLASS II	Oculus Pentacam AXL Wave recalled by Oculus Optikgeraete	Oculus Optikgeraete	Lead & Heavy Metals	Nationwide
6 Sep 2023Device	CLASS II	Oculus Myopia Master recalled by Oculus Optikgeraete	Oculus Optikgeraete	Lead & Heavy Metals	Nationwide
6 Sep 2023Device	CLASS II	Oculus Pentacam AXL recalled by Oculus Optikgeraete	Oculus Optikgeraete	Lead & Heavy Metals	Nationwide
7 Sep 2022Device	CLASS II	Pentacam HR recalled by Oculus Optikgeraete	Oculus Optikgeraete	Device Malfunction	37 states
7 Sep 2022Device	CLASS II	Pentacam AXL Wave recalled by Oculus Optikgeraete	Oculus Optikgeraete	Device Malfunction	37 states
7 Sep 2022Device	CLASS II	Pentacam AXL recalled by Oculus Optikgeraete	Oculus Optikgeraete	Device Malfunction	37 states

All oculus optikgeraete recalls, newest first

7 total

Reported	Class	Recall	Company	Reason	Where
6 Sep 2023Device	CLASS II	Oculus Pentacam AXL Wave recalled by Oculus Optikgeraete	Oculus Optikgeraete	Lead & Heavy Metals	Nationwide
6 Sep 2023Device	CLASS II	Oculus Myopia Master recalled by Oculus Optikgeraete	Oculus Optikgeraete	Lead & Heavy Metals	Nationwide
6 Sep 2023Device	CLASS II	Oculus Pentacam AXL recalled by Oculus Optikgeraete	Oculus Optikgeraete	Lead & Heavy Metals	Nationwide
7 Sep 2022Device	CLASS II	Pentacam HR recalled by Oculus Optikgeraete	Oculus Optikgeraete	Device Malfunction	37 states
7 Sep 2022Device	CLASS II	Pentacam AXL Wave recalled by Oculus Optikgeraete	Oculus Optikgeraete	Device Malfunction	37 states
7 Sep 2022Device	CLASS II	Pentacam AXL recalled by Oculus Optikgeraete	Oculus Optikgeraete	Device Malfunction	37 states
28 Feb 2018Device	CLASS II	Oculus Pentacam AXL recalled by Oculus Optikgeraete	Oculus Optikgeraete	Device Malfunction	CA, FL

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.