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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.

FDA Recall Z-0246-2023 · Posted 2022-11-17

Recalling FirmNovapproach Spine LLC
Recall StatusTerminated
Product CodeOVD
Date Initiated2022-10-12
Date Terminated2026-04-01
Product Quantity6 devices

Reason for Recall

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

Firm 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.

Root Cause

Nonconforming Material/Component

Distribution Pattern

US Nationwide distribution in the states of CA and NY.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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