Steris Corporation: Medical Device Recall in 2021 - (Recall #: Z-0788-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 2, 2020

Date Posted: January 13, 2021

Recall Number: Z-0788-2021

Event ID: 86942

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

Status: Terminated

Product Quantity: 98 cases

Code Information:

Lot Number: 200407A, 200707A

Distribution Pattern:

Nationwide Foreign:

Voluntary or Mandated:

Voluntary: Firm initiated