fda
6 records
FDA Device Recall: Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage:
2020-06-10
Class II — Potential for disengagement of the Varian Style Type-S Extension during patient repositioning. The risk associated with the disengagement of the extension could be a patient fall if the pa...
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FDA Device Recall: CIVCO Solstice(TM) SRS Immobilization System, Part Numbers: a) CHS03, b) CHS04
2019-06-26
Class II — There is a potential for movement of the Solstice Tilting Head Fixation System during patient setup and/or treatment.
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FDA Device Recall: Protura Software which utilizes Elekta's iCOM interface: MT6XSM1.4.0, MT6XSM1.4.
2018-02-28
Class II — When an error message remains displayed and is not cleared in the Protura software with the Elekta pedestal coordinates, moving the pedestal could cause the Protura software to not update w...
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FDA Recall: Med Tec Inc — Class II
20150121
The product (wool wrist loop) was manufactured 7cm shorter than product specifications. | Product: Civco, MTSR02 Shoulder Retractor with Sherpa Wrist Loops Kit with Base, Non-sterile re-usable wool w
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FDA Device Recall: Civco, MTSR02 Shoulder Retractor with Sherpa Wrist Loops Kit with Base, Non-ster
2015-01-21
Class II — The product (wool wrist loop) was manufactured 7cm shorter than product specifications.
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FDA Device Recall: Civco, MTSR03 Shoulder Retractor with Wrist Loops Kit with Base, plus two pairs
2015-01-21
Class II — The product (wool wrist loop) was manufactured 7cm shorter than product specifications.
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ny_corps
1 records
NY Corp: MED. TEC. INTERNATIONAL INC.
2014-03-18
DOMESTIC BUSINESS CORPORATION | County: Suffolk | Jurisdiction: New York
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