Z-2050-2014 Class II Terminated

Recalled by Zimmer, Inc. — Warsaw, IN

FDA device recall Z-2050-2014 was initiated by Zimmer, Inc. on Jun 25, 2014 and is designated Class II. Reason for recall: Zimmer Dental is conducting a voluntary recall of a single lot of the Tapered Screw-Vent Implant, Catalog Number TSVT6B13, Lot number 62284006, due to a potential crack in the cap of the outer vial. The recall status is terminated (terminated Oct 30, 2014). Affected quantity: 129 units.

Recall Details

Product Type
Devices
Report Date
Jul 23, 2014
Initiation Date
Jun 25, 2014
Termination Date
Oct 30, 2014
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
129 units

Product Description

Zimmer Dental Tapered Screw-Vent Implant, Catalog TSVT6B13, Lot 62284006

Reason for Recall

Zimmer Dental is conducting a voluntary recall of a single lot of the Tapered Screw-Vent Implant, Catalog Number TSVT6B13, Lot number 62284006, due to a potential crack in the cap of the outer vial.

Distribution Pattern

Nationwide Distribution.

Code Information

Catalog Number TSVT6B13, Lot Number 62284006. 5-year expiration. January 2018.

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-2050-2014
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 26, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.