FDA recall record

Globus Medical MAGEC 2 Rod, 5.0mm 90mm Standard recall — FDA Z-1657-2025

Devices for the affected lot were not assembled according to product specifications. The distraction rod outer diameter was assembled with a 5.5mm rod…

Class IIclassification
Z-1657-2025official record ID
Apr 30, 2025report date

Recall record at a glance

Official recordZ-1657-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmGlobus Medical, Inc.
Report dateApr 30, 2025
Recall initiation dateApr 3, 2025
Quantity1 unit
LocationWest Norriton, PA, United States

Official product description

MAGEC 2 Rod, 5.0mm 90mm Standard; Version/Model: MC2-5090S;

Why the product was recalled

Devices for the affected lot were not assembled according to product specifications. The distraction rod outer diameter was assembled with a 5.5mm rod versus the required 5.0mm.

Distribution information

US Nationwide distribution in the state of AR.

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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