Stryker iBur 3.0mm Diamond Match Head, Distal Bend - intended to cut bone in the following manne...

FDA Recall #Z-2730-2024 — Class II — July 24, 2024

Recall #Z-2730-2024 Date: July 24, 2024 Classification: Class II Status: Completed

Product Description

Stryker iBur 3.0mm Diamond Match Head, Distal Bend - intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-107-030D

Reason for Recall

Potential for the product to exhibit temperatures higher than specification where the bur shank meets the distal bushing. Temperatures higher than specification may lead to the potential for minor tissue/structure damage or tissue/structure damage from thermal injury which may need medical/surgical intervention.

Recalling Firm

Stryker Corporation — Portage, MI

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

2507 units

Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Canada, France, Hong Kong, India, Italy, Japan, Japan, Netherlands, South Korea, Spain, Sweden, Taiwan, United Kingdom.

Code Information

GTIN: 07613327509229 Lot Numbers: 22334017 23047017 23095017 23198017

Status

Completed

Voluntary / Mandated

Voluntary: Firm initiated