Encore Medical (DJO Surgical) is recalling 146 units of the RSP Glenoid Baseplate, 30mm P2 Porous Coated shoulder device (Part Number 508-32-204). The recall was initiated because the coating hex on the device did not properly engage with surgical tools, specifically the Straight Mod Hexdriver and the Hex Head Screw Driver. This manufacturing defect was identified by the firm and affects products distributed across 17 U.S. states and Puerto Rico.
If the surgical screwdriver cannot properly engage with the device during a shoulder replacement procedure, it can lead to surgical delays, difficulty seating the implant, or the need for alternative surgical instruments.
Manufacturer Notification and Return
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
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Sources: FDA iRES · Raw API Response
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