RecallRadar

FDA Device recall Z-1324-2022

EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion i…

On 2022-07-13 the FDA classified a Class II recall of EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion i… by Depuy Spine, citing 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….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1324-2022
ClassificationClass II
Statusongoing
Initiated2022-05-20
Published2022-07-13
Last updated2026-09-13 11:56 UTC
CompanyDepuy Spine
DistributionUS

Product

EIT CIF cage, H 7mm, 8degree, S- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients with cervical disc disease (DDD) Part Number: CUI8070S

Reason

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

Identifiers

code_infoUDI-DI: 04260557770573 Lot Number: E20CL0637

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Other recalls by Depuy Spine

All Depuy Spine recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1324-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.