medical Class II Updated 2023-08-30

Medicrea International recalls IMPIX ALIF S/A, REF number B15241415; intervertebral fusio

Recalled Product

IMPIX ALIF S/A, REF number B15241415; intervertebral fusion device - lumbar


Hazard / Issue

There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: GTIN 03613720264439, Lot Numbers: 18I0824, 19L0046
View official government recall

Looking for safe alternatives?

Browse certified-safe products in this category on Amazon →