Z-0094-2015 Class II Terminated

Recalled by Zimmer, Inc. — Warsaw, IN

FDA device recall Z-0094-2015 was initiated by Zimmer, Inc. on Oct 1, 2014 and is designated Class II. Reason for recall: The affected products are missing polar boss threads. The recall status is terminated (terminated Mar 2, 2015). Affected quantity: 19.

Recall Details

Product Type
Devices
Report Date
Oct 29, 2014
Initiation Date
Oct 1, 2014
Termination Date
Mar 2, 2015
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
19

Product Description

Continuum Acetabular System Trabecular Metal Shell with Multi Holes, Porous 68mm, Prosthesis, Hip, Semi-Constrained, Metal/Polymer

Reason for Recall

The affected products are missing polar boss threads.

Distribution Pattern

Worldwide Distribution: US (nationwide) in the states of : IA, CA, NC, AL, WA, FL, TN, MA, AZ, TX, UT, and NV; and Internationally to Japan.

Code Information

Part Number: 00-8757-068-02; Lot Number: 62207029

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-0094-2015
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.