FDA Recall Open, Classified

Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description: Total cervical disc replacement Component: No

Recall: Z-1426-2026 · Initiated December 31, 2025

Recall

Recall Number
Z-1426-2026
Event Number
98282
Firm
Centinel Spine, Inc.
FEI Number
3007494564
Product Code
MJO
Status
Open, Classified
Root Cause
Process control
Initiated
December 31, 2025
Posted
February 17, 2026
Address
900 Airport Rd, Ste 3b, West Chester, PA, 19380-3416

Description

Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description: Total cervical disc replacement Component: No

Reason

Products were mislabeled as the 6mm product but included the 5 mm product.

Action

On or around December 31, 2025 Phone calls were made to customers to notify them of the recall. Follow-up URGENT PRODISC C SK US IMPLANT LARGE 6MM DEVICE RECALL letters were also emailed to customers. Actions to be taken: We request that you review your inventory and return any units in your possession of this impacted lot number. We recommend monitoring any patient that has received the recalled device for any unexpected device-related symptoms throughout the regularly scheduled check-in procedures. Actions to Be Taken by Centinel Spine: Centinel Spine intends to remove all remaining implants effected by this recall from the market and issue a replacement product with corrected labeling for any remaining products in the Distributors possession that are subject to this recall.

Distribution

US Nationwide distribution in the states of AL, CA, CO, LA, NY, OR, TN, TX.

Quantity

20 units