Devices

Device Recall Vascular closure device

Model / Serial
OEM Catalog number 610130.
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
No
Distribution
Distributed in DC and the states of CO, CA, FL, TX, and AR.
Product Description
Medical Device Exchange Angio-Seal VIP Platform/Vascular Closure Device 6F; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number 610130. || EXP (repackager), St. Jude Medical (OEM) || Device, hemostasis, vascular
Manufacturer
EXP Pharmaceutical Services Corp
1 Event
- Recall of Device Recall Vascular closure device

Manufacturer

EXP Pharmaceutical Services Corp

Manufacturer Address
EXP Pharmaceutical Services Corp, 48021Warm Springs Boulevard, Fremont CA 94539
Manufacturer Parent Company (2017)
Abry Partners Inc.
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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