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Medicrea International recalls IMPIX ALIF, REF numbers: a) B15111209, b) B15111212, c) B15111409, d) B15111412; intervertebral fusion devic
Recalled August 30, 2023 · FDA recall Z-2453-2023 · 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
11 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, REF numbers: a) B15111209, b) B15111212, c) B15111409, d) B15111412; intervertebral fusion device - lumbar
Manufacturer(s)
Medicrea International
Made in
France
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →