Reported Apr 10, 2024 · Ongoing

Exactech Equinoxe REVERSE SHOULDER, 38mm Humeral Liner: a) +0mm, Item Number 320-38-00, b) +2.5mm, Item Number…

Exactech, 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: Exactech, Inc. · 2320 Nw 66th Ct · Gainesville, FL · 32653-1630

Is this the product you have?

  • Exactech Equinoxe REVERSE SHOULDER, 38mm
  • Humeral Liner
    • a) +0mm
    • Item Number 320-38-00
    • b) +2.5mm
    • Item Number 320-38-03
    • Shoulder Arthroplasty
Lot codes and dates
    • a) Item Number 320-38-00
    • UDI/DI 10885862086655
  • Serial Numbers

    3,615 of 3,615 codes

    • 0983038
    • 0983044
    • 0983058
    • 1033005
    • 1034649
    • 0983051
    • 1032990
    • 1032983
    • 1032992
    • 1092744
    • 1092666
    • 1092747
    • 1030253
    • 1092653
    • 1092748
    • 0983081
    • 1032991
    • 1034629
    • 1034621
    • 1092680
    • 1030248
    • 1032986
    • 1032994
    • 1034627
    • 1092678
    • 1034630
    • 1034619
    • 0983085
    • 1032998
    • 0983043
    • 1092651
    • 1087764
    • 0983049
    • 1034639
    • 1030256
    • 0983074
    • 1034645
    • 1092655
    • 1092661
    • 1092669
    • 0983066
    • 1033002
    • 1034625
    • 1034623
    • 1034607
    • 1034609
    • 1034601
    • 1092636
    • 0983047
    • 1030255
    • 1032997
    • 1092771
    • 0983042
    • 1032995
    • 0983060
    • 0983075
    • 0983056
    • 0983063
    • 0983039
    • 0983079
Amount recalled
66646 units

This recall covers 24 products

The agency filed one notice per product. You are reading one of them; the other 23 are below.

11 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags that did not contain an additional oxygen barrier layer consisting of Ethylene Vinyl Alcohol (EVOH).

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

Data as of Sep 19, 6:21 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.