FDA recall Z-0789-2021

Steris Corporation · Class II · device

Product

Vis-U-All High Temperature Tubing 9"x100'. One roll per box; 10 boxes per case 6 rolls/cs Model Number: 881091

Reason for recall

Purple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) 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

Distribution

Nationwide Foreign:

Key facts

Status
Terminated
Initiation date
2020-12-02
Report date
2021-01-13
Termination date
2022-06-21
Voluntary/Mandated
Voluntary: Firm initiated
Location
Mentor, OH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0789-2021