Medtronic Sofamor Danek USA Inc Medtronic Bone Void Filler, Large - Product Usage: is an injectable, moldable and biocompatible calcium phosphate bone void filler. The single-use Medtronic Bone Void Filler Kit contains the necessary components for mixing of the bone void filler. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic Bone Void Filler, Large - Product Usage: is an injectable, moldable and biocompatible calcium phosphate bone void filler. The single-use Medtronic Bone Void Filler Kit contains the necessary components for mixing of the bone void filler.
Brand
Medtronic Sofamor Danek USA Inc
Lot Codes / Batch Numbers
Product number: C07B, GTIN: 00813845020511, Lot Number: 1127302
Products Sold
Product number: C07B; GTIN: 00813845020511; Lot Number: 1127302
Medtronic Sofamor Danek USA Inc is recalling Medtronic Bone Void Filler, Large - Product Usage: is an injectable, moldable and biocompatible cal due to Product may not maintain its setting characteristics for the labeled shelf-life duration. Use may lead to longer time for product to set at the time o. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product may not maintain its setting characteristics for the labeled shelf-life duration. Use may lead to longer time for product to set at the time of implantation which may increase the required surgical and anesthesia time for the patient. If the device seeps or creeps from its intended position prior to setting and creates incomplete void or gap filling, possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.
Recommended Action
Per FDA guidance
Medtronic notified customers on about 04/24/2020 via "URGENT: Voluntary Market Removal (Recall)" letter. Customers were informed that Medtronic was notified by Skeletal Kinetics LLC that product that may not maintain its setting characteristics for the labeled shelf-life duration of the product, which may lead to a longer period of time required for the product to set at the time of implantation. Instructions included to not use the product and locate and removed the impacted product from inventory, complete the provided Customer Confirmation Form and return it via email to rs.sdmriskmgt@medtronic.com, and contact your Medtronic Sales Representative to coordinate the return and replacement of affected product.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026