Devices

Device Recall Synthes Slipped Capital Femoral Epiphysis System

Model / Serial
Parts 03.207.001 and 03.207.008 with lot numbers: Part # Lot # 03.207.001 PE00376 PE00439 PE01391 PE01329 PE01412 PE00504 03.207.008 PE00440 PE00377 PE00513 PE01475 PE01691
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
USA Nationwide Distribution
Product Description
Slipped Capital Femoral Epiphysis System || Product Usage: Intended for fracture fixation of large bones and large bone fragments and for slipped capital femoral epiphysis, pediatric femoral neck fractures, intercondylar femur fractures and sacroiliac joint disruptions.
Manufacturer
Synthes USA HQ, Inc.
1 Event
- Recall of Device Recall Synthes Slipped Capital Femoral Epiphysis System

Manufacturer

Synthes USA HQ, Inc.

Manufacturer Address
Synthes USA HQ, Inc., 1302 Wrights Ln E, West Chester PA 19380-3417
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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