International Medical Devices Database

Manufacturer Address
CareFusion 213, LLC, 1550 Northwestern Drive, El Paso TX 79912-8000
Manufacturer Parent Company (2017)
Becton, Dickinson and Company
Source
USFDA
1 Event
- Recall of Device Recall Sepp

One device in the database

Device Recall Sepp

Model / Serial
Tincture Packaged: Product Number 260619 and Product ID D086353; Tincture 3,000 Bulk: Product Number 260520 and Product ID D086353.
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
USA Nationwide Distribution
Product Description
Sepp, Compound Benzoin Tincture Packaged and Tincture 3,000 Bulk. || Product Usage: Preoperative skin product

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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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CareFusion 213, LLC

One device in the database

Device Recall Sepp