Exactech recalls Equinoxe Core Instrument Kit (KIT-311X) due to potential missing cross-pin in impactor handle. Affected units sold with UDI-DI 1088586:166. No remedy specified in recall notice.
Impactor handle may be missing cross-pin
Exactech is recalling Equinoxe Core Instrument Kit (model KIT-311X) because the impactor handle might have a missing cross-pin. This could lead to improper function or damage during use. The recall affects all units with the specific UDI-DI number.
The impactor handle may have a missing cross-pin, which could cause the handle to become unstable or malfunction during use. This might lead to improper tool function or potential damage to surgical equipment.
Users of the Equinoxe Core Instrument Kit (KIT-311X) with UDI-DI number 10885862559166 are affected. Medical professionals using this surgical tool are most at risk.
Check for the model number KIT-311X on the product. Affected units have the UDI-DI number 10885862559166. The recall covers all units sold with this specific identifier.
Verify the model number and UDI-DI number on your Equinoxe Core Instrument Kit to confirm if it is affected.
The recall notice does not specify any remedy.
Affected units have the UDI-DI number 10885862559166.
Check for the model number KIT-311X and the UDI-DI number 10885862559166 on the product.
We’ve drafted a message you can send Equinoxe to request your refund or repair — edit it as you like.
Subject: Recall Z-1510-2026 — Equinoxe Equinoxe Hello, I own a Equinoxe that is covered by recall Z-1510-2026 from Equinoxe. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
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