PERMA-HAND™ Silk Suture Recall Over Alcohol-Based Tubing Fluid

Source: Health Canada · Canada

Areazine synthesizes this Health Canada recall directly from Health Canada's official public data feed. See our methodology for full source attribution and refresh cadence.

Ethicon LLC is recalling one lot of PERMA-HAND™ Silk Suture after determining it was incorrectly manufactured with an unapproved alcohol-based tubing fluid.

The full picture behind this Health Canada recall

This notice was issued by Health Canada on September 25, 2026 and geographically references Canada. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - Product & Food Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.

A quick skim tells you whether this affects you directly; a closer read tells you more. Check the scope, the source, and how recent the record is, then weigh it against related notices rather than treating any single one as a trend.

Before acting, the primary agency source is available to check alongside this summary. Its related labels are recall, product-safety, health-canada, MedicalDevice.

What Happened

Ethicon determined that PERMA-HAND™ Silk Suture subject to this recall was incorrectly manufactured with an alcohol-based tubing fluid in the primary packaging. This tubing fluid is an isopropyl alcohol (IPA), diethylaminoethanol (DEAE), and sodium benzoate solution previously used in the manufacture of a different suture product. Up to 80% of the impacted lot may have had the alcohol-based tubing fluid. Tubing fluid is not a material approved for use in the manufacture of PERMA-HAND™ Silk Suture.

Which Products Are Affected

PERMA-HAND™ Silk Suture, model or catalogue number N271H, lot or serial number RLBDPJ.

What You Should Do

No specific consumer action steps are provided in the recall notice.

Why This Matters

The recall addresses the use of an unapproved material in the manufacture of the suture product.

Source

Health Canada

Original source: Health Canada Official Notice ↗

All Product & Food Recalls →

Comparable nationwide notices (length or severity timing) 8

Beyond this Health Canada recall's own category, Areazine surfaces two nationwide peer sets: length-matched and severity/date-matched notices from elsewhere in the archive, distinct from the same-feed Related list above.

Frequently Asked Questions

What people usually ask about a notice like this one.

What is this Health Canada recall about? ▾
Ethicon LLC is recalling one lot of PERMA-HAND™ Silk Suture after determining it was incorrectly manufactured with an unapproved alcohol-based tubing fluid.
Which agency issued this alert? ▾
This alert was issued by Health Canada. The original notice is available at the source link at the bottom of this article.
How severe is this alert? ▾
This alert is classified as "medium" severity. Stay informed and follow agency guidance.
What area is affected? ▾
This alert affects Canada. Check with Health Canada for the most current geographic scope.
Where can I find more Product & Food Recalls updates? ▾
Browse the full Product & Food Recalls feed on Areazine at areazine.com/ca/recalls/ for the latest updates from Health Canada and other agencies.