Medical Device Data System
General Hospital · 21 CFR 880.6310
A medical device data system (mdds) is a device that is intended to provide one or more of the following uses, without controlling or altering the functions or parameters of any connected medical devices: (i) the electronic transfer of medical device data; (ii) the electronic storage of medical device data; (iii) the electronic conversion of medical device data from one format to another format in accordance with a preset specification; or (iv) the electronic display of medical device data. (2) An MDDS may include software, electronic or electrical hardware such as a physical communications medium (including wireless hardware), modems, interfaces, and a communications protocol. This identification does not include devices intended to be used in connection with active patient monitoring.
Recent MDR events
2,981 adverse event reports on file
- OR1 AIR SYSTEM - NO SMARTSCREENJul 31, 2026InjuryKarl Storz Se & Co. Kg9610617-2026-01741
- UNKNOWN FOTA SFTWRJul 9, 2026MalfunctionMedtronic Minimed2032227-2026-202994
- AQUREJul 9, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00070
- AQUREJul 9, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00074
- AQUREJul 7, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00071
- AQUREJul 2, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00068
- AQUREJul 2, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00069
- UNKNOWN FOTA SFTWRJun 24, 2026MalfunctionMedtronic Minimed2032227-2026-195905
- PKG SYNK 4K WIRELESS RECEIVERMay 22, 2026MalfunctionStryker Endoscopy-san Jose0002936485-2026-00324
- PKG SYNK 4K WIRELESS TRANSMITTERMay 21, 2026MalfunctionStryker Endoscopy-san Jose0002936485-2026-00317
Event type breakdown
Recalls
24 recall events for this product code
- Radiometer Medical ApSOpen, ClassifiedApr 17, 2023
AQURE REF 933-599
Due to potential software issue that may result in patient mix-up information.
Z-1394-2023 · View FDA record ↗ - Biomerieux IncOpen, ClassifiedMar 2, 2023
MYLA comprises AST Filters in conjunction with VITEK MS; middleware which connects microbiology laboratory instruments for ID/AST and blood culture activities
For users with MYLA V4.8.X / V4.9 that use VITEK MS to identify organisms as part of their workflow, AST filter rules that have been activated are not always being applied to AST results when sending the results to the clinician.
Z-1201-2023 · View FDA record ↗ - Pentax of America IncTerminatedOct 23, 2020
9372HD Digital Capture (ver. 1.1.0 + w/ 9263 endoPortal),
There is an intermittent software issue that could affect the systems, in which an exam video for one patient (Patient A) might be copied to another patient (Patient B). This does not occur at the time the user performs and initially reviews an exam; it is not evident until a follow-up review occurs.
Z-0292-2021 · View FDA record ↗ - Pentax of America IncTerminatedOct 23, 2020
9310HD Digital Video Capture Module with software version 3.4.0 or higher configured with 9263 endoPortal
There is an intermittent software issue that could affect the systems, in which an exam video for one patient (Patient A) might be copied to another patient (Patient B). This does not occur at the time the user performs and initially reviews an exam; it is not evident until a follow-up review occurs.
Z-0293-2021 · View FDA record ↗ - Beckman Coulter Inc.TerminatedDec 15, 2016
MicroScan LabPro Data Management System.
Beckman Coulter has received and confirmed reports of an intermittent and unexpected behavior when loading new panels into a WalkAway instrument using LabPro Data Management System version 4.42. The issue could cause workflow interruption with a potential of delaying reporting results due to the inability to begin processing new panels.
Z-0768-2017 · View FDA record ↗ - Beckman Coulter Inc.TerminatedSep 23, 2015
MicroScan LabPro Information Manager System, Version 1.0 to Version 4.11, Catalog No. 10714149, 10714150. Intended to manage both microbial identification (ID)
The software incorrectly allows the operator to manually edit the carbohydrate substrates when manually reading dried overnight gram negative panels with an ID Hold status.
Z-2809-2015 · View FDA record ↗ - Maquet Medical Systems USATerminatedJan 16, 2015
TEGRIS System manufactured by MAQUET GMBH in Germany
The wrong movement results on the MAGNUS OR table. The button commands on the TEGRIS touchscreen for Lower Leg Up and Upper Leg Down are switched in the software for the integration with the MAGNUS operating table system.
Z-0993-2015 · View FDA record ↗ - Horiba Instruments IncTerminatedDec 23, 2014
Lite DM (Lite Data Manager)
HORIBA Medical is informing all HORIBA Medical Lite DM customers using software version 2.0.0.19 and lower of a software bug related to the potential for results received being applied to the wrong order in the Lite DM Worklist. This bug has not been seen in software versions above V2.0.0.19 IMPACT: Potential for results received being applied to the wrong order in the Lite DM Worklist. The is
Z-0856-2015 · View FDA record ↗ - Philips Healthcare Informatics, Inc.TerminatedMay 21, 2014
Philips XRE, the dictation editor system included in the Philips XIRIS 8.1.50
When using XIRIS Rio version (8.1.50.0) in conjuncture with iSite PACS a synchronization error can occur and if not noticed, information for the incorrect patient may be displayed
Z-1646-2014 · View FDA record ↗ - Maquet Cardiovascular Us Sales, LlcTerminatedSep 25, 2013
TEGRIS system
MAQUET has identified a potential issue that might occur because of the lack of an emergency stop button on a secondary touch screen display on the TEGRIS System.
Z-2275-2013 · View FDA record ↗
Registered firms
344 firms currently registered for this product code
Carl Zeiss Meditec Ag (oberkochen)
OBERKOCHEN Baden-Wurttemberg, DE
Volk Optical Inc.
Mentor, OH, US
Biocells Discoveries Internacional (biocells)
Quito Pichincha, EC
Sanusom Operating Company, Inc.
Brentwood, TN, US
Sibel Health Inc.
Chicago, IL, US
Arthrex California Technology, Incorporated
Santa Barbara, CA, US
Creation Technologies Ltd
Burnaby British Columbia, CA
Fysicon Bv
Oss Noord-Brabant, NL
Stairway Interactive, Llc
Chicago, IL, US
Imalogix Llc
Bryn Mawr, PA, US
Plexus Corp.
Bathgate West Lothian, GB
Philips Medizin Systeme Boeblingen Gmbh
BOEBLINGEN Baden-Wurttemberg, DE
Nobel Biocare C/o Medicim Nv
Mechelen Antwerpen, BE
Ups Supply Chain Solutions, Inc.
Louisville, KY, US
Biomerieux Sa
MARCY L ETOILE Rhone, FR
Zhejiang Yigao Medical Technology Co., Ltd.
Hangzhou Zhejiang, CN
Resonance Of America, Inc
New York, NY, US
Equitar Technologies, Inc.
La Jolla, CA, US
Arthrex Logistic Center Canada
London Ontario, CA
Agilent Technologies Singapore (international) Pte Ltd.
Singapore North East, SG
Health Data Works
Ponte Vedra Beach, FL, US
Arthrex, Inc.
Ave Maria, FL, US
Cloudphysician.ai
Wilmington, DE, US
Abiomed, Inc.
DANVERS, MA, US
Fisher & Paykel Healthcare, Inc.
IRVINE, CA, US
510(k) clearances
1 clearances for this product code