# FDA recall Z-3208-2017

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

## Product

IMPRESSION CAP CONT 3.5MM, REF ZOCIMP3A;    MPRESSION CAP CONT 3.5MM, REF ZOCIMP3S;    IMPRESSION CAP CONT 4.5MM ANG, REF ZOCIMP4A;    IMPRESSION CAP CONT 4.5MM, REF ZOCIMP4S;    IMPRESSION CAP,CONT,5.5MM, ANG, REF ZOCIMP5A;    IMPRESSION CAP, CONT, 5.5MM, REF ZOCIMP5S;    MPRESSION CAP, CONT, 6.5MM,ANG, REF ZOCIMP6A;    IMPRESSION CAP, CONT, 6.5MM, REF ZOCIMP6S

## 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-3208-2017
- **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-3208-2017

## Citation

> AI Analytics. FDA recall Z-3208-2017. Retrieved 2026-06-04 from https://api.ai-analytics.org/recall/Z-3208-2017. Source: US FDA. Licensed CC0.

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