Corflex
Corflex appears in FDA public data with 7 recalls, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-0574-2016, Class II) was initiated on November 12, 2015.
Summary
- Total Recalls
- 7
- 510(k) Clearances
- 0
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0574-2016 | Class II | Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 Post-Operative Knee Brace is indicate | November 12, 2015 |
| Z-0576-2016 | Class II | HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038 Post-Operative Knee Brace is indicat | November 12, 2015 |
| Z-0580-2016 | Class II | CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative Knee Brace is indicated f | November 12, 2015 |
| Z-0577-2016 | Class II | ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075 Post-Operative Knee Brace is i | November 12, 2015 |
| Z-0578-2016 | Class II | BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087 Post-Operative Knee Brace is | November 12, 2015 |
| Z-0575-2016 | Class II | CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011 Post-Operative Knee Brace is indi | November 12, 2015 |
| Z-0579-2016 | Class II | ADV ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-231 Post-Operative Knee Brace is indica | November 12, 2015 |