FDA recall record

Medtronic Sofamor Danek USA Endoskeleton" TCS Interbody System with Titan nanoLOCK" Surface recall — FDA Z-0086-2022

Engraving on implants may not match what is listed on the pouch labels.

Class IIclassification
Z-0086-2022official record ID
Oct 20, 2021report date

Recall record at a glance

Official recordZ-0086-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedtronic Sofamor Danek USA Inc.
Report dateOct 20, 2021
Recall initiation dateSep 2, 2021
Quantity9 units
LocationMemphis, TN, United States

Official product description

Endoskeleton" TCS Interbody System with Titan nanoLOCK" Surface Technology, NanoLock, 6 Deg, Interbody, Medium, 10mm

Why the product was recalled

Engraving on implants may not match what is listed on the pouch labels.

Distribution information

Distribution in US: CA, MN, MO, NC, NV, NY, OH, OK, OR, PA, SC, SD, WA, WV

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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