Limacorporate recalls specific PRIMA TT Glenoid Monoblock baseplates with potential for loosening due to manufacturing defects. Affected models include D.25mm and D.28mm versions with various wedge angles. Consumers should check product codes and contact Limacorporate for details.
Potential for baseplate peripheral holes to be out of specification due to a manufacturing issue, which could lead to loosening of the implant, or the screw moving from its original position.
Limacorporate is recalling specific PRIMA TT Glenoid Monoblock baseplates that may loosen due to a manufacturing issue. This could cause the implant to shift or screws to move, potentially leading to complications after surgery.
The baseplate peripheral holes may be out of specification because of a manufacturing defect. This could cause the implant to loosen or the screw to shift from its intended position, potentially affecting surgical stability.
Orthopedic patients who received one of the recalled PRIMA TT baseplate models during surgery. Patients with the specific product codes listed in the recall are most at risk.
Check if your PRIMA TT Glenoid Monoblock baseplate has a product code starting with 1975.14.500, 1975.14.800, or similar codes listed in the recall. The baseplate may have a diameter of 25mm or 28mm with specific wedge angles.
Look for the product code on your baseplate, which starts with 1975.14 and includes a unique number like 08033390244824.
Reach out to Limacorporate directly for confirmation of your product and instructions on next steps.
The affected baseplates have product codes starting with 1975.14.500, 1975.14.800, or similar codes listed in the recall. They include specific sizes like 25mm and 28mm with various wedge angles.
Check your product code against the list provided in the recall and contact Limacorporate for further instructions.
The recall states a potential for loosening or screw movement, but it does not specify a risk of serious injury in normal use. The hazard level is low risk.
We’ve drafted a message you can send Limacorporate to request your refund or repair — edit it as you like.
Subject: Recall Z-0726-2024 — Limacorporate Limacorporate Hello, I own a Limacorporate that is covered by recall Z-0726-2024 from Limacorporate. 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.
