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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 8 of 8 Results
510(K) Number: K113707
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Product Description
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Recall
Class
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FDA Recall
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Protexis Neoprene Surgical Glove, Size 5.5 This powder-free sterile light brown colored surgeons ... 2 12/19/2018 Cardinal Health 200, LLC
Protexis Neoprene Surgical Glove, Size 6.0 This powder-free sterile light brown colored surgeon... 2 12/19/2018 Cardinal Health 200, LLC
Protexis Neoprene Surgical Glove, Size 6.5 This powder-free Surgeon s glovessterile light brown c... 2 12/19/2018 Cardinal Health 200, LLC
Protexis Neoprene Surgical Glove, Size 9.0 This powder-free sterile light brown colored surgeons ... 2 12/19/2018 Cardinal Health 200, LLC
Protexis Neoprene Surgical Glove, Size 7.5 This powder-free sterile light brown colored surgeons ... 2 12/19/2018 Cardinal Health 200, LLC
Protexis Neoprene Surgical Glove, Size 8.0 This powder-free sterile light brown colored surgeons ... 2 12/19/2018 Cardinal Health 200, LLC
Protexis Neoprene Surgical Glove, Size 8.5 This powder-free sterile light brown colored surgeons ... 2 12/19/2018 Cardinal Health 200, LLC
Protexis Neoprene Surgical Glove, Size 7.0 This powder-free sterile light brown colored surgeons ... 2 12/19/2018 Cardinal Health 200, LLC
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