Canary Medical recalls Canturio Smart Extension (CSE) implant component with model 43-5570-030-14 due to incorrect labeling. This device is part of Zimmer Persona knee system.
Due to labeling error. Product incorrectly labeled.
Canary Medical is recalling Canturio Smart Extension (CSE) implants with model number 43-5570-030-14 because they were incorrectly labeled. These implants are used with Zimmer Persona knee systems and are single-use medical devices.
The product was incorrectly labeled, meaning the labeling does not match the actual product. This could cause confusion for medical professionals during surgery, but it does not pose a direct safety risk to patients.
Patients who have received the Canturio Smart Extension implant with model number 43-5570-030-14 as part of Zimmer Persona knee surgery are affected. The risk is low since this is a labeling error, not a safety issue.
Check for model number 43-5570-030-14 on the implant. The product is part of Zimmer Persona knee system and sold as a single-use sterile component.
Look for model number 43-5570-030-14 on the implant packaging or device.
No, this is a labeling error, not a safety hazard. The product is safe to use but needs correct labeling.
Contact Canary Medical directly for assistance with the recall.
Check the model number on your implant packaging; affected units have model 43-5570-030-14.
We’ve drafted a message you can send Canturio to request your refund or repair — edit it as you like.
Subject: Recall Z-2099-2025 — Canturio Canturio Hello, I own a Canturio that is covered by recall Z-2099-2025 from Canturio. 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.
