Device Recall Model 6000 CMS, CMS IOD, or Plus Ambulatory Infusion Pump

Model / Serial
Serial Numbers for all affected units: 100074 to 210458
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution --- including USA and countries of Australia, Croatia, Germany, Italy, New Zealand, and South Africa.
Product Description
Model 6000 CMS, CMS IOD, or Plus Ambulatory Infusion Pump, Model Number: 360-1101
Manufacturer
Curlin Medical Llc
1 Event
- Recall of Device Recall Model 6000 CMS, CMS IOD, or Plus Ambulatory Infusion Pump

Manufacturer

Curlin Medical Llc

Manufacturer Address
Curlin Medical Llc, 15751 Graham St, Huntingtn Bch CA 92649-1630
Manufacturer Parent Company (2017)
Moog 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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