FDA recall Z-0992-2018
Zimmer Biomet, Inc. · Class II · device
Product
DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty
Reason for recall
Product may contain the presence of melted sterile packaging upon opening.
Distribution
US in the state of Texas
Key facts
- Status
- Terminated
- Initiation date
- 2017-06-30
- Report date
- 2018-03-21
- Termination date
- 2018-04-13
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Warsaw, IN, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0992-2018