Reported Nov 25, 2020 · Terminated
Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium
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?
- Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium
- Lot codes and dates
- Catalog 314-13-33
- Serial Numbers
6259572625957362595756259577625957862595796259583625958462595876259588625959062595916259592625959462595956132993613299461329956132996613299761329986132999613300061330026133003613300561330086133009613301061330116133013613301461330176133020613302161330236133029613303061330316133032
- Amount recalled
- 40 devices
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
The product may be mislabeled.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Exactech, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.