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Product Recalls & Refunds MN

Smiths Medical ASD Inc.: Pneupac paraPAC plus 310 ventilator kit with PEEP and

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: There is a potential for inadvertent tidal volume knob movement from the original setting when set at high (1000-1500 mL) and low (70-150 mL) settings.. Recalled by Smiths Medical ASD Inc.. Distribution: Worldwide. Classification (Class I — serious health hazard). Affected lots/dates: All serial numbers. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location MN
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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