DePuy Spine, Inc. FDA Recalls

2 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autograft when used as an Class IIMay 20, 2022Label on the Outer Carton does not match the labels on the O	Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Pa	Class IIDevices	May 20, 2022
EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autograft when used as an Class IIMay 20, 2022Label on the Outer Carton does not match the labels on the O	Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Pa	Class IIDevices	May 20, 2022