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Medicrea International recalls IMPIX C+, REF numbers: a) B20240104, b) B20240105, c) B20240106, d) B20240107, e) B20240205, f) B2024020
Recalled August 30, 2023 · FDA recall Z-2460-2023 · 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
0 (US)
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 C+, REF numbers: a) B20240104, b) B20240105, c) B20240106, d) B20240107, e) B20240205, f) B20240206, g) B20240207, h) B20240208; intervertebral fusion device - cervical
Manufacturer(s)
Medicrea International
Made in
France
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →