Devices

Device Recall Synthes In Situ Bender Cutter Kit Sterile Wide

Model / Serial
All lots.
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution.
Product Description
Synthes In Situ Bender/Cutter Kit-Wide-Sterile. Catalog Number 530.521S.
Manufacturer
Synthes USA (HQ), Inc.
1 Event
- Recall of Device Recall Synthes In Situ Bender Cutter Kit Sterile Wide

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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Disclaimer

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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