Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K012695 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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The Reprocessed Mitek Arthroscopic Wand is considered a soft tissue ablators. Soft tissue ablators a... | 2 | 03/13/2012 | Stryker Sustainability Solutions, Inc. |
Arthrocare 3.6 mm Right Angle - Reprocessed Sterile device -- Orthopedic Arthroscope. | 2 | 09/19/2008 | Ascent Healthcare Solutions, Inc. |
Mitek Angled Side Effect Electrode - Reprocessed Sterile device -- Orthopedic Arthroscope. | 2 | 09/19/2008 | Ascent Healthcare Solutions, Inc. |
Mitek 3.5 mm Side Effect Electrode - - Reprocessed Sterile device -- Orthopedic Arthroscope. | 2 | 09/19/2008 | Ascent Healthcare Solutions, Inc. |
Mitek Angled Side Effect Electrode - Reprocessed Sterile device -- Orthopedic Arthroscope. | 2 | 09/19/2008 | Ascent Healthcare Solutions, Inc. |
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