Steris Recalls Vis-U-All Pouches Due to Ink Migration Defects
Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches 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 recall is classified as Low severity because the source text explicitly describes the issue as causing 'cosmetic defects' and ink transference, with no mention of adverse health consequences, injuries, or functional failure of the sterilization process.
Plain-English summary
Steris Corporation is recalling Vis-U-All High Temp 7.5"x13" Self Seal Pouches (Model # 884713, Lot # 161237A and #170237A). The recall involves 127 units distributed nationwide in the United States. These pouches are used by healthcare providers to enclose and seal medical devices for steam sterilization.
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 and consumers should stop using the affected pouches and contact Steris Corporation for further instructions or a refund. The affected lots are specifically identified as #161237A and #170237A.
The recalled product
- Product
- Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box; 4 boxes per case 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 designe
- Manufacturer
- Steris Corporation
- Affected units
- 127
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# 884713 Lot# 161237A and #170237A
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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