Skeletal Kinetics recalls

Skeletal Kinetics has 49 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 27 Jan 2021. The most frequent reason is device malfunction.

Total recalls49since 2015
Last 12 months0reported
Class I00% of total
Ongoing0latest 27 Jan 2021

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 49 100%Class III 0 0%

Why skeletal kinetics is recalled

By year

All skeletal kinetics recalls, newest first

49 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIOsteoVation, Inject, Bone Filler Kits 10cc recalled by Skeletal KineticsSkeletal KineticsOtherNationwide
DeviceCLASS IIOsteoVation, Inject Bone Filler Kits, 5cc recalled by Skeletal KineticsSkeletal KineticsOtherNationwide
DeviceCLASS IISkaffold Renu Flow, 5cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIExactech Ossilix Form (mx), 5cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIExactech Ossilix Form (mx), 10cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIOsteovation Ex, 3cc, Impact Formula recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIAcumed Impact 5cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIAcumed Impact 10cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIOsteovation, 5cc, Inject Formula recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IISk Skaffold Impress 10cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IISkaffold Renu Flow, 10cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIOsteovation, 3cc, Impact Formula recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IICraniosculpt Flow, 10cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIOsteovationex, Inject 3cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IICraniosculpt, Flow 5cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IICraniosculpt, Cmf Impact, 5CC, Product Number: C-CMF5CC recalledSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIMedtronic Bone Void Filler, Small recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IICraniosculpt Flow, Ous, 5CC Product Number: C-FLOW5CC-Ous recalledSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IICraniosculpt C, 10cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IICraniosculpt C, 3cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIOsteovationex 2cc Inject Formula recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IICraniosculpt C, 5cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIOsteovation, 10cc, Inject Formula recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IISkaffold Flow, 3CC and Skaffold Flow (MX) 3CC recalledSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IISkaffold Cmf Impress (mp), 5cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIAcumed Callos Inject 3cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIAcumed Callos Inject 10cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIOsteovation Rmx 5cc recalled by Skeletal KineticsSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IIOsteovation Impact 10CC and Osteovation, 10CC recalledSkeletal KineticsDevice MalfunctionNationwide
DeviceCLASS IICraniosculpt Flow, 10CC, Product Number: C-FLOW10CC-Can recalledSkeletal KineticsDevice MalfunctionNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.