medical Class II Updated 2020-07-22

Skeletal Kinetics, Llc recalls SKAFFOLD FLOW (MX) 5CC. Product Number: SKMX-FL05, UDI: 813

Recalled Product

SKAFFOLD FLOW (MX) 5CC. Product Number: SKMX-FL05, UDI: 813845020894 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. Callos Bone Void Filler is indicated only for bony voids or gaps that are not intrinsic to the stability of the bony structure. The product provides a bone void filler that resorbs and is replaced by bone during the healing process.


Hazard / Issue

Bone void filler kits may not maintain its setting characteristics for the labeled shelf-life duration. Use may increase the required surgical and anesthesia time for the patient or possible longer-term health consequences could include incomplete bone formation or lack of bone formation, delayed union, or nonunion.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot Numbers: 1136227, 1137065.
View official government recall

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