Steris Corporation: Medical Device Recall in 2021 - (Recall #: Z-0787-2021)

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 4"x100'. One roll per box; 10 boxes per case 10 rolls/cs Model Number: 881041

Product Classification:

Class II

Date Initiated: December 2, 2020

Date Posted: January 13, 2021

Recall Number: Z-0787-2021

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: 65 units

Code Information:

Lot Number: 200406A

Distribution Pattern:

Nationwide Foreign:

Voluntary or Mandated:

Voluntary: Firm initiated