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Other Medical Devices

🏥 Medical Devices 15,809 recalls

On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All Pouches may migrate following steam processing causing cosmetic defects on the exterior of the pouch and in some instances, transference of the ink onto the device(s) contained within the pouch.

Jun 15, 2017 Other Medical Devices Nationwide View Details →

On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All Pouches may migrate following steam processing causing cosmetic defects on the exterior of the pouch and in some instances, transference of the ink onto the device(s) contained within the pouch.

Jun 15, 2017 Other Medical Devices Nationwide View Details →

Integrity R1.2

Elekta Limited

Class I - Dangerous

Potential for positional errors following automatic table movement (ATM).

Nov 20, 2017 Other Medical Devices Nationwide View Details →

If the tilt-drive motor has an intermittent connection or broken encoder or sensor wire there is a risk of unintended or unpredictable device motion while the CT system is homing the axis at startup or preparing for a scan.

Sep 26, 2017 Other Medical Devices Nationwide View Details →

Ultra Renew Plus

Accord Media

Class I - Dangerous

Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation

Dec 4, 2017 Other Medical Devices Nationwide View Details →

On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All Pouches may migrate following steam processing causing cosmetic defects on the exterior of the pouch and in some instances, transference of the ink onto the device(s) contained within the pouch.

Jun 15, 2017 Other Medical Devices Nationwide View Details →

On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All Pouches may migrate following steam processing causing cosmetic defects on the exterior of the pouch and in some instances, transference of the ink onto the device(s) contained within the pouch.

Jun 15, 2017 Other Medical Devices Nationwide View Details →

Alcon is conducting this Voluntary Medical Device Recall for a specific lot (2060953H) of its 25+ TOTALPLUS Vitrectomy Pak due a potential that a 23GA ULTRAVIT probe may be included within the 25+ TOTALPLUS Vitrectomy Pak, instead of a 25+ ULTRAVIT probe.

Jan 12, 2018 Other Medical Devices View Details →

On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All Pouches may migrate following steam processing causing cosmetic defects on the exterior of the pouch and in some instances, transference of the ink onto the device(s) contained within the pouch.

Jun 15, 2017 Other Medical Devices Nationwide View Details →

On June 15, 2017, STERIS identified that the purple ink located on the outside label of Vis-U-All Pouches may migrate following steam processing causing cosmetic defects on the exterior of the pouch and in some instances, transference of the ink onto the device(s) contained within the pouch.

Jun 15, 2017 Other Medical Devices Nationwide View Details →