Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented
Zimmer Manufacturing B.v.'s record for this product code
Recent MDR events
606 adverse event reports on file
- CPT 12/14 STEM SIZE 1 COCRJun 23, 2026Injury0002648920-2026-00120
- BONE SCREW SELF-TAPPING 30 MM LENGTH 6.5 MM DIA.Jun 9, 2026Injury0002648920-2026-00099
- BONE SCREW SELF-TAPPING 30 MM LENGTH 6.5 MM DIA.Jun 9, 2026Injury0002648920-2026-00100
- BONE SCREW SELF-TAPPING 30 MM LENGTH 6.5 MM DIA.Jun 9, 2026Injury0002648920-2026-00101
- BONE SCREW SELF-TAPPING 30 MM LENGTH 6.5 MM DIA.Jun 9, 2026Injury0002648920-2026-00102
- BONE SCREW SELF-TAPPING 35 MM LENGTH 6.5 MM DIA.Jun 9, 2026Injury0002648920-2026-00103
- BONE SCREW SELF-TAPPING 35 MM LENGTH 6.5 MM DIA.Jun 9, 2026Injury0002648920-2026-00104
- BONE SCREW SELF-TAPPING 25 MM LENGTH 6.5 MM DIA.Jun 9, 2026Injury0002648920-2026-00105
- BONE SCREW SELF-TAPPING 40 MM LENGTH 6.5 MM DIA.Jun 9, 2026Injury0002648920-2026-00106
- CEM REV/CALCAR ST SZ 17X230MMMay 19, 2026Injury0002648920-2026-00079
Recalls
21 recall events for this product code
- TerminatedMay 16, 2016
A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
View FDA record ↗ - TerminatedMar 12, 2016
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
View FDA record ↗ - TerminatedMar 12, 2016
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
View FDA record ↗ - TerminatedMar 12, 2016
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
View FDA record ↗ - TerminatedMar 12, 2016
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
View FDA record ↗ - TerminatedMar 12, 2016
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
View FDA record ↗ - TerminatedMar 12, 2016
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
View FDA record ↗ - TerminatedMar 12, 2016
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
View FDA record ↗ - TerminatedMar 12, 2016
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
View FDA record ↗ - TerminatedMar 12, 2016
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
View FDA record ↗
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Zimmer Manufacturing B.v. under this product code.