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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 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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OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product prov... 2 05/29/2020 Osteomed, LLC
OSTEOVATIONEX 3CC INJECT FORMULA. REF/UDI: 390-0003/00813845020016 - Product Usage: The product prov... 2 05/29/2020 Osteomed, LLC
OSTEOVATIONEX 5CC INJECT FORMULA. REF/UDI: 390-0005/00813845020023 - Product Usage: The product prov... 2 05/29/2020 Osteomed, LLC
OSTEOVATION 5CC INJECT FORMULA. REF/UDI: 390-2005/00813845020054 - Product Usage: The product provid... 2 05/29/2020 Osteomed, LLC
OSTEOVATION 10CC INJECT FORMULA. REF/UDI: 390-2010/00813845020061 - Product Usage: The product provi... 2 05/29/2020 Osteomed, LLC
ACUMED CALLOS INJECT 5CC. Product Number: 65-0005-S, UDI: 813845020238 - Product Usage: Callos is i... 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 3CC. Product Number: 65-0003-S, UDI: 813845020221 - Product Usage: Callos is ... 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
EXACTECH OSSILIX FIL (MX), 10CC. Product Number: 660-02-10, UDI: 813845021013 - - Product Usage: Ca... 2 07/15/2020 Skeletal Kinetics, Llc
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