Medicrea International: Medical Device Recall in 2023 - (Recall #: Z-2454-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 12, 2023

Date Posted: August 30, 2023

Recall Number: Z-2454-2023

Event ID: 92738

Reason for Recall:

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

Status: Ongoing

Product Quantity: 5 units

Code Information:

GTIN 03613720264439, Lot Numbers: 18I0824, 19L0046

Distribution Pattern:

US nationwide

Voluntary or Mandated:

Voluntary: Firm initiated