HS DOMS GMBH
6 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (6)
Devices registered here (1)
- Table, Instrument, Powered, OphthalmicProduct code HRJ (opens in a new tab) · Class I · Ophthalmic · 21 CFR 886.4855
Recalls & enforcement
- Class IIOngoing2021-11-03Malfunction of the automatic laser beam shut-off, the OCT unit might not recognize whether the laser beam is safely switched off
- Class IIOngoing2021-04-15Examination data and patient name may be mixed up when printing or generating a pdf with the interface at Pacific Coast and Laser Institute (PCLI).
- Class IIOngoing2020-11-20Software error -Software REF 615 588 versions 2.0 to 3.3, movement of the focusing is triggered by pressing the button of the footswitch it might occur that the movement does not stop when releasing the button, result in potential risk to the patient's eye
- Class IITerminated2019-07-31software error in the central control unit of the floor stand.
- Class IITerminated2017-01-05There is a possibility for data to be stored under the wrong patient on the DICOM Server following a non-standard workflow.
- Class IITerminated2012-08-17The firm recalled the device after learning of a possible deviation in the stimulus luminance of the Perimeter OCTOPUS 101.
Related
- All facilities operated by HAAG-STREIT HOLDING
- HAAG-STREIT AG (CH)
- HAAG-STREIT UK LTD. (GB)
- HAAG-STREIT USA, INC. (OH)
- Haag-Streit Deutschland GmbH (DE)
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “HS DOMS GMBH (FEI 3015399802) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3015399802-hs-doms-gmbh/
Alerts for HS DOMS GMBH
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.