prodisc C SK, Total cervical disc replacement, medical device, Model/Catalog Number: PDSM5
FDA Recall Z-3212-2024 · Posted 2024-09-24
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Recalling FirmCentinel Spine, Inc.
Recall StatusOpen, Classified
Product CodeMJO
Date Initiated2024-07-18
Product Quantity12 units
Reason for Recall
During the assembly of Prodisc C, a blue discoloration was observed on a Prodisc C inlay. The discoloration is considered a foreign contaminate that may not have been fully evaluated in the manufacturing validations.
Firm Action
Customers were contacted via telephone beginning 7/18/24.
The Centinel Quality team has identified a potential nonconformance on three specific lots in the prodisc c product family.
We are requesting the return of the inventory that is assigned to you.
We will provide replacement inventory proactively to support the business.
Thank you for your support.
In addition, an URGENT - MEDICAL DEVICE Recall Instructions for PRODISC C IMPLANTS notification letter was sent to the distributor.
Required Action: Please retrieve the identified devices and return the affected devices to Centinel Spine
Depth of Recall: This recall should be carried out to the hospital level, including Distributors and Consigned locations
Please acknowledge that you have read the email and enable the Return Receipt. This is necessary to ensure traceability as part of the recall process. If you have any questions, please contact Jessica Staub 484.887.8803.
Root Cause
Process control
Distribution Pattern
US Nationwide distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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