ClearanceBrief
Recall Z-0788-2021 ยท FRG Wrap, Sterilization

Steris Corporation

Vis-U-All High Temperature Tubing 6"x100'. One roll per box; 10 boxes per case 10 rolls/cs Model Number: 881061

DateDec 2, 2020
StatusTerminated
ReasonPurple 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
Root causeProcess control
ActionSteris issued Urgent Medical Device Recall issued 12/2/20 to Distributors and Customers. Letter states reason for recall, health risk and action to take: 1.Please immediately inspect on-hand inventory for Vis-U-All High Temperature Sterilization Pouches and Tubing. For the full list of affected product and associated lots, please reference Attachment A to this letter. 2. Please complete the Medical Device Recall Response Form included with this Customer Notification Letter and destroy any remaining product in inventory. STERIS will coordinate shipment of replacement product upon receipt of th
Quantity98 cases
DistributionNationwide Foreign:
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K153540Safe Secure Sterilization Pouch with Steam and Ethylene Oxide Process Indicators
Safe Secure Packaging Co., Ltd., Aug 4, 2016