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Medicrea International recalls IMPIX ALIF S/A, REF number B15241415; intervertebral fusion device - lumbar
Recalled August 30, 2023 · FDA recall Z-2454-2023 · Medicrea International
Hazard
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch. · FDA Class II
Units
5 units
Sold at
US nationwide
Description
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
Product
IMPIX ALIF S/A, REF number B15241415; intervertebral fusion device - lumbar
Manufacturer(s)
Medicrea International
Made in
France
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →