Limacorporate recalls bone screws that may not match label length. This could lead to improper use in medical procedures. Affected units have specific model numbers and were sold in certain regions.
There is a potential that the length of bone screws identified on labeling may not correspond to the actual length of the screw included.
Limacorporate is recalling bone screws that might not match the length stated on their labels. This could cause improper use during medical procedures if the screws are too short or too long.
The screws might be shorter or longer than labeled, which could lead to improper fixation in bone structures. This might cause complications during surgery or after the procedure if the screws aren't the correct size.
Medical professionals using these screws for surgeries or orthopedic procedures are most at risk. Patients receiving these screws during surgery could be affected if the screws don't match the label length.
Check for the model number 2100099 on the packaging or label. The screws have a diameter of 6.5mm and height of 20mm, and are sterile. They were sold with the UDI codes (01)08033390018845 and 2103825.
Look for the model number 2100099 on the packaging or label to confirm if it's affected.
The recall states there's a potential that the screws may not match the label length, which could lead to improper use during medical procedures. However, the hazard is not described as causing serious injury in normal use.
Check for the model number 2100099 on the packaging or label. The screws have a diameter of 6.5mm, height of 20mm, and are sterile with UDI codes (01)08033390018845 and 2103825.
The recall does not specify a remedy, so the official notice does not state what action to take.
We’ve drafted a message you can send Limacorporate to request your refund or repair — edit it as you like.
Subject: Recall Z-0160-2022 — Limacorporate Limacorporate Hello, I own a Limacorporate that is covered by recall Z-0160-2022 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.
