Zimmer, Inc. Identity Shoulder System Resection Planer 35mm Resection Planer Recall

Check Your Product

According to the U.S. Food and Drug Administration (FDA)

Reason for Recall

As stated by FDA

Two planers were found to be unusable during sawbones shoulder training.

Recommended Action

Per FDA guidance

Consignee notification was made to impacted distributors and hospitals beginning December 27, 2022. Consignees are asked to immediately check inventory and quarantine any impacted devices. Return of product is to be made to Zimmer Biomet via an Inventory Return Certification Form. This form shall be completed even if there is no impacted inventory.