Reported Aug 15, 2018 · Terminated
Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism
Smiths Medical ASD Inc.
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: Smiths Medical ASD Inc. · 6000 Nathan Ln N · Minneapolis, MN · 55442-1690
Is this the product you have?
- Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism
- Lot codes and dates
- Barrel Clamp Guide mechanism numberG6000716
- Barrel Clamp Guide lot numbers
P0239588P0321444and P0462421
- Amount recalled
- 276 units
Where it was sold
Why it was recalled
Certain Barrel Clamp Guides may contain a ridge that could potentially lead to spring slippage, resulting in the inability of the pump to recognize a loaded syringe or the pump, misidentifying the size of a loaded syringe.
This product could cause temporary or reversible health problems — stop using it.
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