Z-2365-2018 Class II Terminated
FDA device recall Z-2365-2018 was initiated by Zimmer Biomet, Inc. on May 30, 2018 and is designated Class II. The recall status is terminated (terminated May 28, 2020). Affected quantity: 24.
Recall Details
- Product Type
- Devices
- Report Date
- Jul 11, 2018
- Initiation Date
- May 30, 2018
- Termination Date
- May 28, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 24
Product Description
Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 10; 00-7713-010-00
Distribution Pattern
Products were distributed solely to Japan.
Code Information
62361460 62528141
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2365-2018
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026