Devices

Device Recall Medamicus FlowGuard

Model / Serial
Lot Number W23155
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
The products were distributed to 4 consignees in Georgia, Missouri, New York and North Carolina. Most of the product was shipped to a distributor in New York which probably shipped to other states. There was no direct distribution to foreign or U.S Government accounts.
Product Description
Medamicus FlowGuard 15FR Valved Peelable Introducer Kit, Catalog Number 10532-010
Manufacturer
MedAmicus,Inc
1 Event
- Recall of Device Recall Medamicus FlowGuard

Manufacturer

MedAmicus,Inc

Manufacturer Address
MedAmicus,Inc, 15301 Highway 55 West, Plymouth MN 55447
Source
USFDA

2 devices with a similar name

Learn more about the data here

Device Recall Medamicus FlowGuard

Model / Serial
Lot Number W23152
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
The products were distributed to 4 consignees in Georgia, Missouri, New York and North Carolina. Most of the product was shipped to a distributor in New York which probably shipped to other states. There was no direct distribution to foreign or U.S Government accounts.
Product Description
Medamicus FlowGuard 16 FR Valved Peelable Introducer Kit, Catalog Number 10532-011
Manufacturer
MedAmicus,Inc

Device Recall Medamicus FlowGuard

Model / Serial
Lot Number W24369
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
The products were distributed to 4 consignees in Georgia, Missouri, New York and North Carolina. Most of the product was shipped to a distributor in New York which probably shipped to other states. There was no direct distribution to foreign or U.S Government accounts.
Product Description
Medamicus FlowGuard 16 FR Valved Peelable Venous Introducer, 5 units per shelf box, Part Number 10684-003
Manufacturer
MedAmicus,Inc

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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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