DKK Dai-Ichi Shomei Co., Ltd.: Device Recall

Recall #Z-2619-2024 · 07/09/2024

Class II: Risk

Recall Details

Recall Number
Z-2619-2024
Classification
Class II
Product Type
Device
Recalling Firm
DKK Dai-Ichi Shomei Co., Ltd.
Status
Ongoing
Date Initiated
07/09/2024
Location
Itabashi, Japan
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
822 units

Reason for Recall

The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.

Product Description

Aurora 2 Series, Aurora 7 lighthead; Models: AUR7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure visibility of the surgical site.

Distribution Pattern

Domestic: Nationwide Distribution International: Australia, Canada, Egypt, Hong Kong, Indonesia, Japan, Jordan, Netherlands, New Zealand, Philippines, Singapore, South America, South Korea, Thailand, UAE.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.