FDA recall record

Prodisc C SK recall — FDA Z-1426-2026

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

Class IIclassification
Z-1426-2026official record ID
Feb 25, 2026report date

Recall record at a glance

Official recordZ-1426-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCentinel Spine, Inc.
Report dateFeb 25, 2026
Recall initiation dateDec 31, 2025
Quantity20 units
LocationWest Chester, PA, United States

Official product 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

Why the product was recalled

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

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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