Limacorporate S.p.A recalls Prima TT Genoid Monoblock Reverse TT Baseplate (STERILE R) due to potential peripheral holes being out of specification. All lots are affected.
Due to manufacturing issue, their is a potential for peripheral holes to be out of specification.
Limacorporate S.p.A is recalling all units of the Prima TT Genoid Monoblock Reverse TT Baseplate (STERILE R) because manufacturing issues may cause peripheral holes to be out of specification. This could affect the product's function or safety, though the recall does not specify a risk of serious injury.
The product has peripheral holes that may be out of specification due to a manufacturing issue. This could lead to improper function or performance, but the recall does not indicate a risk of serious injury or harm.
Users of the Prima TT Genoid Monoblock Reverse TT Baseplate (STERILE R) are affected. Those using the product in medical or laboratory settings may be at higher risk due to potential functional issues.
Check for the product name 'Prima TT Genoid Monoblock Reverse TT Baseplate (STERILE R)' and the UDI-DI code 08033390244824. All lots of this product are affected.
Verify the product name and UDI-DI code to confirm if your item is recalled.
The recall does not state a risk of serious injury; it only mentions potential functional issues.
Check for the product name 'Prima TT Genoid Monoblock Reverse TT Baseplate (STERILE R)' and the UDI-DI code 08033390244824. All lots are affected.
The recall does not specify a remedy; you should check product details to confirm if it's affected.
We’ve drafted a message you can send Limacorpor: S.p.A to request your refund or repair — edit it as you like.
Subject: Recall Z-2009-2023 — Limacorpor: S.p.A Limacorpor: S.p.A Hello, I own a Limacorpor: S.p.A that is covered by recall Z-2009-2023 from Limacorpor: S.p.A. 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.
