Class 2 Device Recall Pan Medical US/Zavation ZVplasty

• Date Initiated by Firm: March 25, 2021
• Create Date: June 01, 2021
• Recall Status: Terminated on March 20, 2023
• Recall Number: Z-1762-2021
• Recall Event ID: 87661
• Product Classification: Cement, bone, vertebroplasty - Product Code NDN
• Product: ZVplasty System, 15mm, Part Numbers: a) VCF-1015-2 b) VCF-1015-2A. For use in Orthopedic / spinal procedures.
• Code Information: a) VCF-1015-2, Lot Numbers: 13814ZV, 10950ZV, 11694ZV, 10953ZV, 10779ZV, 10588ZV, 13664ZV, 13469ZV, 13519ZV, 10825ZV, 13885ZV, 12989ZV, 10933ZV, 13758ZV, 14107ZV, 14206ZV, 14680ZV, 14022ZV, 11603ZV, 10505ZV b) VCF-1015-2A, Lot Numbers: 10515ZV, 14197ZV, 14114ZV, 14113ZV, 14024ZV, 14023ZV, 13641ZV, 13471ZV, 13325ZV
• Recalling Firm/ Manufacturer: Zavation; 220 Lakeland Pkwy; Flowood MS 39232-9552
• For Additional Information Contact: Quality Department; 601-919-1119
• Manufacturer Reason for Recall: Products distributed as sterile may not have been adequately sterilized
• FDA Determined Cause: Vendor change control
• Action: Zavation initially notified their consignees of the problem by email beginning on 03/24/2021 and requested they quarantine the product. The firm sent a subsequent email beginning on 04/13/2021 requesting the return of the product. The recall is being conducted to the user level.
• Quantity in Commerce: 195 units
• Distribution: US nationwide distribution.
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.