Home › MOTUS GI MEDICAL TECHNOLOGIES LTD › MOTUS GI Endoscopy Cart (Accessory)
MOTUS GI Endoscopy Cart (Accessory)
MOTUS GI MEDICAL TECHNOLOGIES LTD · Model EN-CRT-03-0 · UDI-DI 05060513700168
10
510(k) clearances
84,519
Adverse events (63 deaths)
25
Recalls
77
Facilities
Description
Endoscopy Cart Accessory used with the MOTUS GI Workstation
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-01-11 | Olympus Corporation of the Americas | Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in tempera |
| 2024-01-11 | Olympus Corporation of the Americas | Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in tempera |
| 2024-01-11 | Olympus Corporation of the Americas | Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in tempera |
| 2023-10-16 | Aizu Olympus Co., Ltd. | Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in |
| 2023-10-16 | Aizu Olympus Co., Ltd. | Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in |
| 2023-10-16 | Aizu Olympus Co., Ltd. | Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in |
| 2023-10-16 | Aizu Olympus Co., Ltd. | Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in |
| 2023-10-16 | Aizu Olympus Co., Ltd. | Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in |
| 2023-10-02 | Olympus Corporation of the Americas | Sterilization failures when devices are sterilized per the Reprocessing Manual due to lack of drying time for the endoscope channel. |
| 2023-09-25 | Aizu Olympus Co., Ltd. | Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endo |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.