FDA Recall Terminated

OneLIF Torque Limiting Adapter, AO to 1/4 SQ, 2.25Nm Limit, Catalog #015-010-0000, a component of NovApproach Spine OneLIF Interbody System instrument kit, Catalog #OneLIF INS.

Recall: Z-0246-2023 · Initiated October 12, 2022

Recall

Recall Number
Z-0246-2023
Event Number
91016
Firm
Novapproach Spine LLC
FEI Number
3020307303
Product Code
OVD
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
October 12, 2022
Posted
November 17, 2022
Terminated
April 1, 2026
Address
13900 Tech City Cir, Ste 300, Alachua, FL, 32615-6091

Description

OneLIF Torque Limiting Adapter, AO to 1/4 SQ, 2.25Nm Limit, Catalog #015-010-0000, a component of NovApproach Spine OneLIF Interbody System instrument kit, Catalog #OneLIF INS.

Reason

The torque limiting adapter may not stay locked inside of the ratcheting handle once fully engaged.

Action

The recalling firm issued letters dated 10/10/2022 via email on 10/12/2022. The email briefly described the product to be recalled, the issue, and what the consignee needed to do. The letter, which was also mailed to the consignee via certified mail, return receipt, on 10/12/2022, describes the product, reason for recall, and provides the actions necessary to complete the product removal. The actions include immediately discontinuing use of the torque adapter, remove it from the consigned OneLIF INS-Instrument Kits(s), receive a replacement OneLIF Torque adapter Lot 106607 to add back to the kit, and receive a return label to return the torque adapter to the location provided. No response form was enclosed. The recalling firm will be coordinating with a third-party logistics provider to track the return of the product for quarantine and storage until all product has been returned.

Distribution

US Nationwide distribution in the states of CA and NY.

Quantity

6 devices