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Devices
Device Recall ONQ PainBuster
Model / Serial
Lot numbers: 662449 & 662742
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
I-Flow ON-Q PainBuster (100 ml, 2 mI/hr) Pump, PM012, Lot #662449 and 662742
Manufacturer
I-Flow Corporation
1 Event
Recall of Device Recall ONQ PainBuster
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Manufacturer
I-Flow Corporation
Manufacturer Address
I-Flow Corporation, 20202 Windrow Dr, Lake Forest CA 92630-8152
Source
USFDA
One device with a similar name
Learn more about the data
here
Device Recall ONQ PainBuster with OnDemand
Model / Serial
6A4171 (exp. MAR 2009), 694133 (exp. FEB 2009), 654920 (exp. OCT 2008), 5A4732 (exp. MAR 2008), 584699 (exp. JAN 2008)
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, USA and Australia
Product Description
ON-Q PainBuster with OnDemand (270 ml, 2 ml/hr + 5 ml bolus /60 min refill), Model PMB01, I-Flow Corporation, Lake Forest, CA 92630 U.S.A.
Manufacturer
I-Flow Corporation
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