Reported Nov 25, 2020 · Terminated
Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, 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 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
- Lot codes and dates
- Catalog 314-13-23
- Serial Numbers
69 of 69 codes
626274662627476262748626274962627506262751626275362627546262756626275762627586262759626276062627616262762626276361427766142777614277961427806142782614278361427856142787614278861427906142792614279361427946142795614279661427986142801614280261428036142804613033461303356130336613034061303416130343613034461303476130352613035361303556130356613035761303586130361613036561303666130367613036861472876147294614729761472986147299
- Amount recalled
- 69 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.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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