Presource ®kits Containing Teleflex Pilling® Wecksorb Neurosponge

Recall Summary Presource Kits containing Teleflex Pilling Wecksorb Neurosponge are being recalled across Canada due to a device performance issue. These kits are medical devices used in surgical and clinical settings. The recall is classified as Class II, meaning the product could cause temporary or reversible adverse health effects.

Product

Presource ®Kits containing Teleflex Pilling® Wecksorb Neurosponge

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-07-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f6bca7ac-f950-4c4f-b827-6b6908aefbcf