Medical DeviceMay 4, 2016
Corin USA Trinity Acetabular System Product Usage - Total Hip Replacement recall — FDA Z-1526-2016
Potential for abrasion of the sterile barrier pouches of the new packaging system.
Class IIFDA: TerminatedCorin USA Limited
Recall history in this database
Classification mix: Class II: 3.
Medical DeviceMay 4, 2016
Corin USA Trinity Acetabular Shell Product Usage Total Hip Replacement recall — FDA Z-1528-2016
Potential for abrasion of the sterile barrier pouches of the new packaging system.
Class IIFDA: TerminatedCorin USA Limited
Medical DeviceMay 4, 2016
Corin USA Trinity Acetabular Shell Product Usage: Total Hip Replacement recall — FDA Z-1527-2016
Potential for abrasion of the sterile barrier pouches of the new packaging system.
Class IIFDA: TerminatedCorin USA Limited
Understanding this recall history
This page summarizes recall records in which the official source identifies Corin USA Limited as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.