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Ritter
MIDMARK CORPORATION · Model 255-002 · UDI-DI 00841709106743
10
510(k) clearances
401
Adverse events
5
Recalls
92
Facilities
Description
The Ritter 9' Single Ceiling Mount LED Procedure Light is intended to be used in medical environments where illumination is required for medical use during external examinations and procedures.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-10-13 | MRIMed Inc. | Due to battery component overheating while charging resulting in melting of internal components and causing smoke. |
| 2017-04-21 | Stryker Communications | The exam light may have a tolerance issue with the adapter assembly, which could potentially not allow the snap ring to be seated correctly. If this is the case, there could be in |
| 2016-11-18 | Ohmeda Medical | Certain power cords could overheat. The affected power cords were manufactured by Electric-Cord and are referred to as Taller Bridge power cords. The overheating of the power cord |
| 2013-07-25 | Stryker Communications | Potential incomplete final weld on the drop tube flange. |
| 2004-02-19 | Burton Medical Products Corp | Pivot joint on these ceiling mount lights may fail and lights may fall onto patients. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.