Devices

Device Recall SIMS Portex

Model / Serial
Lot Number: K223373
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
AZ, CA, CO, CT, FL, GA, IN, MA, NJ, NY, TN, TX, WI
Product Description
PER-FIT Percutaneous Dilational Tracheostomy Kit with Specialty Tracheostomy Tube || REF # 511080
Manufacturer
Smiths Medical ASD, Inc.
1 Event
- Recall of Device Recall SIMS Portex

Manufacturer

Smiths Medical ASD, Inc.

Manufacturer Address
Smiths Medical ASD, Inc., 10 Bowman Dr, Keene NH 03431-5043
Manufacturer Parent Company (2017)
Smiths Group 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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