Med Tec Recalls
9 recalls on record · January 21, 2015 to June 10, 2020 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 10, 2020Medical DevicesFDA
Med Tec Inc recalls Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient positioni
Hazard: 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 patient is not supported by clinical staff.
June 26, 2019Medical DevicesFDA
Med Tec Inc recalls CIVCO Solstice(TM) SRS Immobilization System, Part Numbers: a) CHS03, b) CHS04 - Product Usage: The Tilting Head Fixati
Hazard: There is a potential for movement of the Solstice Tilting Head Fixation System during patient setup and/or treatment.
February 28, 2018Medical DevicesFDA
Med Tec Inc recalls Protura Software which utilizes Elekta's iCOM interface: MT6XSM1.4.0, MT6XSM1.4.0-1, MT6XSM1.4.0-2, MT6SXM1.4.0-3, MT6XS
Hazard: 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 with the pedestal location and buffers the pedestal movement history.
September 6, 2017Medical DevicesFDA
Med Tec Inc recalls CIVCO Arm Support, REF 106047, distributed as: (a) Rigid Arm Support, Large, Set, Red (PN: 106047) (b) PB2-BDLRL (PN:
Hazard: Rigid Arm Supports (PN: 106015 and 106047), which were used as part of the Posiboard-2 and Posirest, and were distributed as PN: 106015, 106047, 106521, 106522, 109030, and 109040 between Ocotober 2009 and July 2012 may have a height difference of approximately 17mm.
September 6, 2017Medical DevicesFDA
Med Tec Inc recalls CIVCO Arm Support, REF 106015, distributed as: (a) Rigid Arm Support, Standard, Set Red (PN: 106015) (b) Rigid Adj.
Hazard: Rigid Arm Supports (PN: 106015 and 106047), which were used as part of the Posiboard-2 and Posirest, and were distributed as PN: 106015, 106047, 106521, 106522, 109030, and 109040 between Ocotober 2009 and July 2012 may have a height difference of approximately 17mm.
June 22, 2016Medical DevicesFDA
Med Tec Inc recalls Protura Robotic Couch System Software, versions 1.6.1 (Part Number MT6XSM1.6.1), 1.7.0 (Part Number MT6XSM1.7.0), and 1.
Hazard: When using the recalled product in split shift mode, the non-sub-millimeter positioning has been found to be inconsistent with the setting parameters.
September 23, 2015Medical DevicesFDA
Med Tec Inc recalls CIVCO Shoulder Retractors, Reusable non-sterile hand grip, REF 302070, packaged 1 set per box, RX. For use in patien
Hazard: The wrist straps used for positioning the patient are too long
January 21, 2015Medical DevicesFDA
Med Tec Inc recalls Civco, MTSR03 Shoulder Retractor with Wrist Loops Kit with Base, plus two pairs of wrist loops (nylon and sherpa), Non-s
Hazard: The product (wool wrist loop) was manufactured 7cm shorter than product specifications.
January 21, 2015Medical DevicesFDA
Med Tec Inc recalls Civco, MTSR02 Shoulder Retractor with Sherpa Wrist Loops Kit with Base, Non-sterile re-usable wool wrist strap, REF: 20S
Hazard: The product (wool wrist loop) was manufactured 7cm shorter than product specifications.