Z-2760-2015 Class II Terminated
FDA device recall Z-2760-2015 was initiated by Biomet 3I, LLC on Jul 29, 2015 and is designated Class II. Reason for recall: MUCC2, non-hexed, castable abutment cylinders, has been labeled and distributed as a MUCC1C, hexed, castable abutment cylinders for this one lot only. The recall status is terminated (terminated May 16, 2016). Affected quantity: 61 pieces.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 23, 2015
- Initiation Date
- Jul 29, 2015
- Termination Date
- May 16, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 61 pieces
Product Description
UCLA Abutment Hexed Castable Cylinder 3.4mm Are accessories to endosseous dental implant to support a prosthetic device in a partially or completely edentulous patient.
Reason for Recall
MUCC2, non-hexed, castable abutment cylinders, has been labeled and distributed as a MUCC1C, hexed, castable abutment cylinders for this one lot only.
Distribution Pattern
Worldwide Distribution including Italy and Uruguay.
Code Information
Model # MUCC1C LOT # 1186054
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2760-2015
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026