Overview of recall records associated with Limacorporate S.p.A, including dates, categories and classifications where available.
Classification mix: Class II: 7.
There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.
There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.
Due to a potential difference in mechanical behavior between the implanted device and tool(s) used during revision surgery.
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…
Shoulder glenoid fossa prosthesis was manufactured without tantalum markers so in the absence of the markers, on already implanted devices, a correct radiographic assessment of the hybrid…
There is a potential that the length of bone screws identified on labeling may not correspond to the actual length of the screw included.
There is a potential that the length of bone screws identified on labeling may not correspond to the actual length of the screw included.
This page summarizes recall records in which the official source identifies Limacorporate S.p.A as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
