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Terminated

Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system

FDA Recall Z-0570-2021 · Posted None

Recalling FirmZimmer Biomet, Inc.
Recall StatusTerminated
Product CodeNKB
Date Initiated2020-11-17
Date Terminated2021-07-27
Product Quantity57,715 units

Reason for Recall

Zimmer Biomet is conducting a medical device correction to update the Instructions for Use (IFU) and the Surgical Techniques for the Polaris Spinal System Translation Screw and Cypher MIS Screw System. Users should be aware that changes were made to the contraindications section indicating that the Translation Screws should not be used with a direct current stimulation, as a high probability of construct failure exists when using Translation Screws containing CoCr with direct current simulation system.

Firm Action

On November 17, 2020, the firm distributed Urgent Medical Device Correction letters to customers. Customers were notified that changes were made to the contraindications section indicating the following: "Translation Screws should not be used with a direct current stimulation, as a high probability of construct failure exists when using Translation Screws containing CoCr with direct current simulation system." The updated instruction for use is available electronically at labeling.zimmerbiomet.com, and the updated surgical technique is available electronically at zimmerbiomet.com. Customers were asked to do the following: 1. Review this notification and ensure that affected team members are aware of the contents. 2. Ensure that the most updated instructions for use (IFU) (060505-02 Polaris Spinal System IFU and 14-501697-00 Cypher MIS Screw System IFU) and the surgical techniques (0744.1-US-en-REV1120 Polaris 5.5 Spinal System Surgical Technique Guide, 0746.1-US-en-REV1120 Polaris Spinal System Translation Screw Surgical Technique Guide, and 2075.1-US-en-REV1120 Cypher MIS Screw System Surgical Technique Guide) for the Polaris Spinal System Translation Screw and Cypher MIS Screw Systems are used, effective immediately, for surgeries that require the affected items. a. Access the instruction for use at labeling.zimmerbiomet.com by navigating to key-code 060505-02 and 14-501697-00. b. Access the surgical technique at zimmerbiomet.com by navigating to https://www.zimmerbiomet.com/medical-professionals/spine/product/polaris-5-5-spinal-system.html and https://www.zimmerbiomet.com/medical-professionals/spine/product/cypher-mis-screw-system.html. c. Destroy any previous copies of the instruction for use and surgical technique. Customers are to complete and return the Acknowledgement Form accompanying the notification. If you have further questions or concerns about this recall, please call Zimmer Biomet's customer service at 800-447-3625 betwee

Root Cause

Use error

Distribution Pattern

Domestic distribution nationwide. As direct stimulation devices are only available in the US, this contraindication does not apply to international customers.

Official Source

View FDA Recall →

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

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