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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 →

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 →

Ultra Renew

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 →

Possible sterile barrier breach in the pouch of Affinity NT Cardiotomy Venous Reservoir stand alone uncoated and Affinity NT Cardiotomy Venous Reservoir stand alone Trillium coated products.

Jan 16, 2018 Other Medical Devices View Details →

After multiple reprocessing cycles, the epoxy resin which holds the TCN Electrode in the hub can exhibit signs of damage. In some cases, this damage may result in the inability to fully remove blood and/or tissue residuals prior to cleaning and re-sterilizing the device.

Jul 5, 2017 Other Medical Devices Nationwide View Details →

3-Way Standardbore Stopcock. Product Code: AMS-100.

Vygon MFG, Inc., dba/ Churchill Medical Systems

Class I - Dangerous

Vygon is conducting a voluntary recall of the products and lots listed in this recall, being initiated because our Tyvek supplier has notified Vygon of issues with their product, specifically the Tyvek may not be coated completely causing gaps in the adhesive used to seal the product packaging. This potential lack of adhesive may affect the sterility of the product.

Jul 24, 2017 Other Medical Devices View Details →

FUJIFILM Medical Systems U.S.A., Inc. (FMSU) identified a potential failure with our Mammography system. The acquisition workstations, FDR¿1000AWS, FDR-2000AWS, FDR-3000AWS, and CR¿IR363AWS assign a unique ID number to every image study but very rarely, with the acquisition workstation software versions, VS.O, VS.1, VS.2 , V6.0, V6.1, and V7.0, the system may assign the same ID number to a new set of images that was already assigned to the previous set of images due to the error in ID number generation logic. If an Image with this error (with duplicate ID number) Is transmitted to PACS, it may overwrite the image already stored on PACS.

Aug 4, 2017 Other Medical Devices View Details →

CVC Tray Pediatrics. Product Code: AMS-9335CP-2.

Vygon MFG, Inc., dba/ Churchill Medical Systems

Class I - Dangerous

Vygon is conducting a voluntary recall of the products and lots listed in this recall, being initiated because our Tyvek supplier has notified Vygon of issues with their product, specifically the Tyvek may not be coated completely causing gaps in the adhesive used to seal the product packaging. This potential lack of adhesive may affect the sterility of the product.

Jul 24, 2017 Other Medical Devices View Details →