Reported Sep 2, 2020 · Terminated

ALTERA Spacer ALTERA Spacer, 10x26, 9-13mm, 8¿

Globus Medical, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Globus Medical, Inc. · 2560 General Armistead Ave · Audubon, PA · 19403-5214

Is this the product you have?

    • ALTERA Spacer ALTERA Spacer
    • 10x26
    • 9-13mm
    • 8¿
Lot codes and dates

11 of 11 products

Products covered by this recall
#BarcodesProduct as published
11124.1012
200889095258363Lot # / UDI #: BAX096BE / (01)00889095258363(10)BAX096BE
300889095258363BAX112TE / (01)00889095258363(10)BAX112TE
400889095258363BAX112SE / (01)00889095258363(10)BAX112SE
500889095258363BAX177UE / (01)00889095258363(10)BAX177UE
600889095258363BAX195VE / (01)00889095258363(10)BAX195VE
700889095258363BAX229TE / (01)00889095258363(10)BAX229TE
800889095258363BAX279WE / (01)00889095258363(10)BAX279WE
900889095258363BAX288HE / (01)00889095258363(10)BAX288HE
1000889095258363BAX299GE / (01)00889095258363(10)BAX299GE
1100889095258363BAX367FE / (01)00889095258363(10)BAX367FE
Amount recalled
N/A

This recall covers 22 products

The agency filed one notice per product. You are reading one of them; the other 21 are below.

9 more are in the archive.

Why it was recalled

Specific lots of ALTERA¿ implants have internal components that may have been manufactured using stainless steel rather than the specified cobalt chromium molybdenum alloy.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 19, 2021 · Data as of Sep 19, 5:25 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.