restor3d recalls Veritas Standard Glenoid Baseplate models 1500-1030 and 1500-1035 due to potential improper screw engagement. Affected patients should contact the manufacturer for details.
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.
restor3d is recalling Veritas Standard Glenoid Baseplate models 1500-1030 and 1500-1035 because of a machining error that could cause screws to not engage properly. This may lead to improper shoulder replacement surgery outcomes.
The baseplate has a machining error in the peripheral screw hole that could cause the screws to not engage properly during surgery. This might lead to improper shoulder replacement, but the risk is not immediate or life-threatening.
Patients who received the Veritas Standard Glenoid Baseplate models 1500-1030 or 1500-1035 for reverse total shoulder replacement surgery are affected. Surgeons and medical staff using these specific models are at higher risk.
Check for model numbers 1500-1030 or 1500-1035 on the baseplate. The product was sold as part of the restor3d Reverse Total Shoulder Arthroplasty System.
Reach out to restor3d Inc. for specific instructions on how to handle the recalled baseplate.
No, only the Veritas Standard Glenoid Baseplate models 1500-1030 and 1500-1035 are affected. Patient-specific baseplates are not included.
Contact restor3d Inc. directly for guidance on the next steps.
The recall indicates a potential for improper screw engagement during surgery, but it does not describe immediate risks to patients in normal use.
We’ve drafted a message you can send restor3d to request your refund or repair — edit it as you like.
Subject: Recall Z-2987-2026 — restor3d restor3d Hello, I own a restor3d that is covered by recall Z-2987-2026 from restor3d. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
