Recall Z-1717-2021— Zavation

Class II · Terminated

Class II FDA medical device recall by Zavation, initiated 2021-03-25, terminated 2023-03-20. FDA's recall record names no specific 510(k) clearance for this event. Product: 11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES) CODE: INTVMN-SCDK. For use in Orthopedic / spinal procedures.. Reason: Products distributed as sterile may not have been adequately sterilized.

Recalling firm
Zavation
Classification
Class II
Status
Terminated
Initiated
2021-03-25
Terminated
2023-03-20
Firm location
Flowood, MS, United States

Product description

11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES) CODE: INTVMN-SCDK. For use in Orthopedic / spinal procedures.

Reason for recall

Products distributed as sterile may not have been adequately sterilized

Data sourced from openFDA. This site is unofficial and independent of the FDA.