Devices

Device Recall VERIFY SixCess 270FP Challenge Pack

Model / Serial
Model LCC019, Lot #: 024552A
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution: US (nationwide) including states of: IL, LA, ME, MI, NC, OH, OK, VA, WI & WV; and to the country of: Canada. Product was also shipped to Canada.
Product Description
VERIFY¿ SixCess 270FP Challenge Pack, STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060, 440-354-2600. || The VERIFY¿ SixCess 270FP Challenge Pack is used to monitor steam sterilization loads processed at 270¿F using typical healthcare dynamic air removal steam sterilization cycles.
Manufacturer
Steris Corporation
1 Event
- Recall of Device Recall VERIFY SixCess 270FP Challenge Pack

Manufacturer

Steris Corporation

Manufacturer Address
Steris Corporation, 5960 Heisley Rd, Mentor OH 44060-1834
Manufacturer Parent Company (2017)
Steris 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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