Devices

Device Recall CIVCO ProLok Platform, REF MTSBRT002

Model / Serial
M074130, M092920, M115600, M143230, M165570, M188350, M191650, M207130, M208340, M213570, M218300, M230730, M248840, M248850 and M268010
Product Classification
Radiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA ( nationwide) including the state of PA. and countries of: Canada, China, England, Israel, Italy, Japan, Korea, The Netherlands, Russia, Spain, Sweden, Switzerland and Turkey.
Product Description
CIVCO Pro-Lok Platform, REF MTSBRT002. Firm name on label is CIVCO, Orange City, Iowa || Product Usage: The recalled product is intended to support and aid in positioning a patient during radiologic and other medical procedures.
Manufacturer
Civco Medical Instruments Inc
1 Event
- Recall of Device Recall CIVCO ProLok Platform, REF MTSBRT002

Manufacturer

Civco Medical Instruments Inc

Manufacturer Address
Civco Medical Instruments Inc, 102 1st St S, Kalona IA 52247-9589
Manufacturer Parent Company (2017)
Roper Technologies 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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