Devices

Device Recall Hand Foot II

Model / Serial
Serial numbers: 39870, 39873, 39874, 39866, 39867, 39871, 39869
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide distribution. US states: IA, IL, MI, NY, PA, and WI. Country: Jordan. There are no government accounts for this recall. There are no Canada accounts for this recall. There are no Mexico accounts for this recall.
Product Description
Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated box. For UV phototherapy treatment.
Manufacturer
National Biological Corp
1 Event
- Recall of Device Recall Hand Foot II

Manufacturer

National Biological Corp

Manufacturer Address
National Biological Corp, 23700 Mercantile Rd, Beachwood OH 44122-5900
Manufacturer Parent Company (2017)
National Biological Corporation
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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