Steris Recalls Vis-U-All High Temperature Tubing Due to Ink Migration
Steris Corporation is recalling Vis-U-All High Temperature Tubing because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The source text explicitly identifies the issue as causing 'cosmetic defects' and ink transference, which aligns with the rubric for cosmetic defects and packaging-only problems.
Plain-English summary
Steris Corporation is recalling 156 units of Vis-U-All High Temperature Tubing (Model # 881091, Lot # 161108A). The product is a high-temperature sterilization pouch used by healthcare providers to enclose and seal medical devices for steam sterilization. The affected units were distributed nationwide in the United States.
The recall was initiated after Steris identified that the purple ink on the outside label of the pouches may migrate following steam processing. This migration can cause cosmetic defects on the exterior of the pouch and, in some instances, result in the transfer of ink onto the medical devices contained within the pouch.
Healthcare providers who have purchased or received this specific lot of Vis-U-All High Temperature Tubing should stop using the product and contact Steris Corporation for instructions on how to return the affected units.
The recalled product
- Product
- Vis-U-All High Temperature Tubing 9"x100'. One roll per box; 10 boxes per case 6 rolls/cs Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is
- Manufacturer
- Steris Corporation
- Affected units
- 156
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Model# 881091 Lot# 161108A
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 29 recalled by Steris Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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