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Prescott’s Wall Mount Surgical Microscope Platform
Prescott's Inc. · Model PMPLP-WM000 - WALL MOUNT · UDI-DI 00850047802002
10
510(k) clearances
473
Adverse events
14
Recalls
76
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-11-21 | Leica Microsystems, Inc. | There is a potential issue resulting in the Power Supply potentially becoming overheated due to internal components overstressing. Consequently, due to the overstressing of the int |
| 2022-11-21 | Leica Microsystems, Inc. | There is a potential issue resulting in the Power Supply potentially becoming overheated due to internal components overstressing. Consequently, due to the overstressing of the int |
| 2020-05-20 | Leica Microsystems, Inc. | Possible unintended interruption of surgical procedures due to equipment shutdown, related to changes in voltage. |
| 2019-07-31 | Haag-Streit USA Inc | software error in the central control unit of the floor stand. |
| 2019-07-31 | Haag-Streit USA Inc | software error in the central control unit of the floor stand. |
| 2019-07-31 | Haag-Streit USA Inc | software error in the central control unit of the floor stand. |
| 2018-09-04 | Leica Microsystems, Inc. | The firm received complaints that the instrument tipped over when the swing arm was fully extended. |
| 2018-06-04 | Leica Microsystems, Inc. | Possible failure of screws which hold the gas spring fixation bracket in place. Due to this failure, the gas spring, which is fixed to the upper part of the parallelogram, cannot |
| 2017-01-01 | Seiler Instr. & Mfg. Co. Inc. | The microscope may tip over if attachments are fully extended in one line and there is an attempt to move the device not by the handles mounted on the post. |
| 2013-04-18 | Carl Zeiss Meditec, Inc. | Carl Zeiss Meditec is conducting a field corrective action for its OPMI Pentero C surgical microscope system. During a routine inspection, one microscope installation was found to |
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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.
