Devices

Device Recall Verify SixCess Challenge Pack

Model / Serial
Model #'s: LCC003, LCC005, LCC014 & LCC310.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA (nationwide) and the countries of Lebanon and Qatar.
Product Description
Verify¿ SixCess Challenge Pack, Model #'s: LCC003, LCC005, LCC014 & LCC310, Mfr. By: Albert Browne, LTD, Chancery House 190 Waterside Rd. Hamilton Industrial Park, Leicester, Leicester, LE5QZ, United Kingdom. || Verify¿ SixCess Challenge Packs are used to confirm that that critical parameters of steam sterilization have been reached within a challenging test pack design. Each challenge pack is also specific to a sterilization temperature and type (i.e. 275¿F 3 minute Prevacuum Cycle).
Manufacturer
Steris Corporation
1 Event
- Recall of Device Recall Verify SixCess Challenge Pack

Manufacturer

Steris Corporation

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