Home / Recalls / Medical Devices
Medicrea International recalls IMPIX MANTA+, REF numbers: a) B20171743, b) B20171753, c) B20171763, d) B20171773, e) B20171943, f) B201719
Recalled August 30, 2023 · FDA recall Z-2462-2023 · 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
N/A
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 MANTA+, REF numbers: a) B20171743, b) B20171753, c) B20171763, d) B20171773, e) B20171943, f) B20171953, g) B20171963, h) B20171973, i) B20172253, j) B20172263, k) B20172273; intervertebral fusion device - cervical
Manufacturer(s)
Medicrea International
Made in
France
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →