DePuy Spine, Inc. Recalls

Overview of recall records associated with DePuy Spine, Inc., including dates, categories and classifications where available.

2recall records

Jul 13, 2022latest record date

Jul 13, 2022earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceJul 13, 2022

DePuy Spine EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated recall — FDA Z-1324-2022

Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton

Class IIFDA: OngoingDePuy Spine, Inc.

Medical DeviceJul 13, 2022

DePuy Spine EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated recall — FDA Z-1323-2022

Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton

Class IIFDA: OngoingDePuy Spine, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies DePuy Spine, Inc. 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.