Reported Feb 17, 2016 · Terminated
Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory…
MOOG Medical Devices Group
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MOOG Medical Devices Group · 4314 S Zevex Park Ln · Salt Lake City, UT · 84123-7881
Is this the product you have?
3 of 3 products
| Model / number | Product as published |
|---|---|
340 | Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-therapy and PainSmart pumps. Curlin 4000 |
360 | Curlin 6000, 6000 CMS, and PainSmart IOD |
340-4038. | and Curlin Pump Calibration Set |
- Amount recalled
- 11,472
Where it was sold
- Nationwide
Why it was recalled
Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps manufactured or serviced by MMDG between March 18, 2015 and November 6, 2015 because the master pumps used to calibrate them were out of tolerance and may cause an over delivery of medications and solutions at a rate of 1.2 - 6.8% faster than programmed.
This product could cause temporary or reversible health problems — stop using it.
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