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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 17 of 17 Results
510(K) Number: K051123
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Product Description
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Recall
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FDA Recall
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MEDTRONIC BONE VOID FILLER, LARGE. Product Number: C07B, UDI: 813845020511 - Product Usage: Callos ... 2 07/15/2020 Skeletal Kinetics, Llc
EXACTECH OSSILIX FIL (MX), 5CC. Product Number: 660-02-05, UDI: 813845021006 - Product Usage: Callo... 2 07/15/2020 Skeletal Kinetics, Llc
EXACTECH OSSILIX FIL (MX), 10CC. Product Number: 660-02-10, UDI: 813845021013 - - Product Usage: Ca... 2 07/15/2020 Skeletal Kinetics, Llc
OSTEOVATIONEX, INJECT 3CC. Product Number: 390-0003, UDI: 813845020016 - Product Usage: Callos is i... 2 07/15/2020 Skeletal Kinetics, Llc
ACUMED CALLOS INJECT 3CC. Product Number: 65-0003-S, UDI: 813845020221 - Product Usage: Callos is ... 2 07/15/2020 Skeletal Kinetics, Llc
ACUMED CALLOS INJECT 10CC. Product Number: 65-0010-S, UDI: 813845020245 - Product Usage: Callos is ... 2 07/15/2020 Skeletal Kinetics, Llc
ACUMED CALLOS INJECT 5CC. Product Number: 65-0005-S, UDI: 813845020238 - Product Usage: Callos is i... 2 07/15/2020 Skeletal Kinetics, Llc
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