FDA Recall Open, Classified

W&H Surgical handpiece S-12. For Surgical treatment of dental hard tissue Model Number: 30061000

Recall: Z-1168-2024 · Initiated January 16, 2024

Recall

Recall Number
Z-1168-2024
Event Number
93917
Firm
W & H DENTALWERK BUERMOOS GMBH Ignaz Glaser Strase 53 53 IGNAZ-GLASER-STRASSE BUERMOOS Austria
FEI Number
3003755849
Product Code
KMW
Status
Open, Classified
Root Cause
Labeling False and Misleading
Initiated
January 16, 2024
Posted
February 20, 2024

Description

W&H Surgical handpiece S-12. For Surgical treatment of dental hard tissue Model Number: 30061000

Reason

1:2 speed increasing surgical handpieces have been incorrectly laser marked during production. The specific laser marking should read 1:2, but instead it reads 1:1 on the body of the handpiece

Action

W&H Dentalwerk Burmoos GmbH issued Urgent Medical Device Voluntary Recall Letter on 12/16/23 to Distributors and End Users via email. Letter states reason for recall, health risk and action to take: This recall is carried out to the user level. Please return product to W&H Impex Inc. for disposal within two (2) months after receipt of this notification. Address for removal: W&H Impex Inc. Attn. Mona Miron Regulatory Affairs, Technical Service Manager 6490 Hawthorne Dr, Windsor, ON t +1 800 265 6277 The affected products will be exchanged and replaced by W&H Dentalwerk Brmoos GmbH. Instructions for acknowledgement: Please send back the included return response card. CONTACT INFORMATION: Mona Miron Regulatory Affairs Technical Service Manager W&H Impex Inc 6490 Hawthorne Dr, Windsor, ON t +1 800 265 6277 [email protected]

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Australia, Philippines, Sweden.

Quantity

160 pieces