Z-2144-2014 Class II Terminated
FDA device recall Z-2144-2014 was initiated by Zimmer, Inc. on Jul 17, 2014 and is designated Class II. Reason for recall: Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner vial state "03.7 x 8mm" instead of "04.7 x 8 mm." The recall status is terminated (terminated Feb 6, 2015). Affected quantity: 291 units.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 13, 2014
- Initiation Date
- Jul 17, 2014
- Termination Date
- Feb 6, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 291 units
Product Description
Tapered-Screw Vent Implant, HA, 4.7mmD x 8mmL x 4.5mm, Part No. TSVWH8 Dental implant component.
Reason for Recall
Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner vial state "03.7 x 8mm" instead of "04.7 x 8 mm."
Distribution Pattern
Worldwide Distribution-USA (nationwide) and the countries of Holland, Italy, and Japan.
Code Information
Lot No. 62552804
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2144-2014
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026