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Medicrea International recalls PASS LP, REF numbers: a) B02315535Z, b) B02315540Z, c) B02315545Z, d) B02315550Z, e) B02316535Z, f) B023165
Recalled August 30, 2023 · FDA recall Z-2458-2023 · 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
963 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
PASS LP, REF numbers: a) B02315535Z, b) B02315540Z, c) B02315545Z, d) B02315550Z, e) B02316535Z, f) B02316540Z, g) B02316545Z, h) B02316550Z, i) B02317540Z, j) B02317545Z, k) B02317550Z; intervertebral fusion device - cervical
Manufacturer(s)
Medicrea International
Made in
France
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →