Skip to the content

FDA Medical Device Recalls (openFDA)

Zimmer Dental Inc: THREAD RETRIEVAL DRILL REF 2224

Recall number
Z-3205-2017
Recalling firm
Zimmer Dental Inc
Product
THREAD RETRIEVAL DRILL REF 2224
Status
Terminated
Initiated
2017-07-10
Posted
not on file
Terminated
2019-08-05
Reason
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.
Root cause
Under Investigation by 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.
Quantity
237 products
Distribution
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)
Lot, serial or model codes
lot # 63241114, 63321266, 63426543
510(k) numbers
not on file
PMA numbers
not on file
Product code
DZA
Firm FEI
1038806
Firm city
Carlsbad
Firm state
CA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

Search this register