Skeletal Kinetics, Llc recalls OsteoVation, Inject Bone Filler Kits, 5cc (part number 390-2005, manufacturing lot number 1129957) - Product Usage: The…
- Recall date
- June 6, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0866-2021
- FDA classification
- Class II
- Brand / firm
- Skeletal Kinetics, Llc
- Sold / distributed
- U.S. Nationwide distribution including in the states of TX, NY, FL and AZ.
Why it was recalled
A discrepancy was found between the Mixing Instruction Card and the Instructions for Use for the 5cc and 10 cc bone void filler kits. No customer complaints or reports of injury have been received.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
OsteoVation, Inject Bone Filler Kits, 5cc (part number 390-2005, manufacturing lot number 1129957) - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Get recall alerts
Free email alert whenever Skeletal Kinetics, Llc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Skeletal Kinetics, Llc