THREAD RETRIEVAL DRILL REF 2224
FDA Recall Z-3205-2017 · Posted None
Recalling FirmZimmer Dental Inc
Recall StatusTerminated
Product CodeDZA
Date Initiated2017-07-10
Date Terminated2019-08-05
Product Quantity237 products
Reason for Recall
Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the products were missing supplemental IFUs.
Firm Action
The affected customers are being provided instructions on how to obtain the supplemental IFUs for respective part numbers from appropriate E-labeling website along with a recall notice.
Root Cause
Under Investigation by firm
Distribution Pattern
US, Canada, France, Israel, Hong Kong, Netherlands, Japan, Italy, Belgium, Thailand, Saudi Arabia, Taiwan (Province of China), United Arab Emirates, Panama, Venezuela (Bolivarian Republic of), Chile, Colombia, Australia, Singapore, Costa Rica, Morocco, Trinidad and Tobago, Lebanon, Ecuador, Malaysia, Turkey, Serbia, Pakistan, Korea (the Republic of)
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.