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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K021680
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Product Description
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Recall
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FDA Recall
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Invacare® Pronto® Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare W... 2 08/10/2015 Invacare Corporation
MK5 NX Controller--Wheelchair controller 2 07/22/2014 Invacare Corporation
Pronto M51 Wheelchair, component- seat 3 08/10/2006 Invacare Corporation
Pronto Series Power Wheelchair, model M51. 2 06/17/2005 Invacare Corporation
Pronto Series Power Wheelchair, model M50. 2 06/17/2005 Invacare Corporation
Pronto Series Power Wheelchair, model M61. 2 06/17/2005 Invacare Corporation
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