Urgent Field Safety Notice For Interpulse System By Stryker Instruments-kalamazoo

Summary Stryker Instruments-Kalamazoo has issued an urgent safety notice for the InterPulse System, a medical device distributed in Germany and the EU. The notice is classified as Class I, indicating a serious issue. The specific reason for the safety notice is not detailed in the provided information.

Recalling firm
Stryker Instruments-Kalamazoo
Product
InterPulse System
Reason
Urgent Field Safety Notice for InterPulse System by Stryker Instruments-Kalamazoo
Classification
Class I
Category
medical device recall
Country
Germany
Agency
BFARM
Recall date
2026-10-20
Status
Ongoing
Distribution
Germany / EU

Official recall notice from BFARM

Recall details on Nibble Recalls: https://trynibble.app/recalls/ff70271d-f4f5-4c25-bbb3-93cffab2c233