# FDA recall Z-3207-2017

> **Zimmer Dental Inc** · Class II · device recall initiated 2017-07-10.

## Product

TRY-IN,ABUTMENT, CONT, 3.5X4.5, REF ZOAT34;    TRY-IN, ABUTMENT, CONT, 4.5X5.5, REF ZOAT45;    TRY-IN, ABUTMENT, CONT, 5.7X6.5, REF ZOAT56;    TRY-IN KIT, ABUTMENT, CONT, REF ZOATKIT

## 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.

## 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)

## Key facts

- **Recall number:** Z-3207-2017
- **Recalling firm:** Zimmer Dental Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-10
- **Report date:** 2017-10-04
- **Termination date:** 2019-08-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Carlsbad, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3207-2017

## Citation

> AI Analytics. FDA recall Z-3207-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-3207-2017. Source: US FDA. Licensed CC0.

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