Devices

Device Recall ProSpore

Model / Serial
Lots: PS-673, PS-674, PS-675, PS-675
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
United States, Republic of Korea, Israel, Poland, France, China, Canada, Japan, Singapore, Hong Kong, Jordan
Product Description
ProSpore Biological Indicator Part Numbers: PS-6-50, PS-5-50, PS-4-10, PS-4-50, 3471
Manufacturer
Mesa Laboratories Bozeman Manufacturing Facility
1 Event
- Recall of Device Recall ProSpore

Manufacturer

Mesa Laboratories Bozeman Manufacturing Facility

Manufacturer Address
Mesa Laboratories Bozeman Manufacturing Facility, 625 Zoot Way, Boseman MT 59718
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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