PrimaConnex Tapered Implant TC, SD Internal Connection 3.5… recallZ-0973-2013 · Keystone Dental Inc · initiated Mar 11, 2013
Class II Terminated All recalls posted in March 2013
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Keystone Dental Inc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Mislabeled: Cover screw that was in the package was a WD cover screw and not a SD cover screw as labeled
FDA root cause category: Packaging process control
What the company is doing
Keystone Dental initially called customers on 3/11/13 and forms were completed to document these calls. In addition, a letter sent via Federal Express/or hand delivered to all distributors and customers. Product requested to be returned.
Recall details
- Recall number
- Z-0973-2013
- Recall class
- Class II
- Status
- Terminated
- Initiated by the company
- Mar 11, 2013
- Posted by the FDA
- Mar 20, 2013
- Recalling firm
- Keystone Dental Inc
- Quantity
- 120 units
- Product code
- NDP
- FDA submissions
- K051614
- Distribution
- Worldwide Distribution-USA including DC and the states of CA, FL, IN, MA, MN, NJ, NY, NH, PA, WI, and NY, and the countries of Republic of China, Germany, and France.
Product description
PrimaConnex Tapered Implant TC, SD Internal Connection 3.5 x 10mm Catalog Number: l5613K. Implants in support for fixed bridgework.
Code information (models, lots, serial numbers)
Lot Number: 12857
Other devices under the same FDA submission
53 devices cleared under K051614 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- Prima Implant System 15617KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM379 reports
- Prima Implant System 15618KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM328 reports
- Prima Implant System 15613KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM287 reports
- Prima Implant System 15621KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM270 reports
- Prima Implant System 15619KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM248 reports
- Prima Implant System 15614KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM216 reports
- Prima Implant System 15622KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM181 reports
- Prima 15736KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM151 reports
- Prima Implant System 15615KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM145 reports
- Prima 15741KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM111 reports
- Prima Implant System 15634KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM90 reports
- Prima 15737KKeystone Dental, Inc. · IMPLANT, ENDOSSEOUS, ROOT-FORM87 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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