Biomet recalls Juggerknot Mini Soft Anchors (model 912080) due to incorrect product labels in shipping cartons. This mismatch may cause confusion for users.
The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton are JuggerKnot 1.4mm Short devices.
Biomet is recalling Juggerknot Mini Soft Anchors (model 912080) because the carton labels incorrectly state 1.0mm products when they contain 1.4mm devices. This mismatch could lead to users selecting the wrong product for their needs.
The carton box labels indicate 1.0mm products, but the actual items inside are 1.4mm devices. This mismatch could lead to users selecting the wrong product for their intended use, potentially causing improper application or functionality.
Users who purchased Juggerknot Mini Soft Anchors with model number 912080 from Biomet are affected. Those using these anchors for medical applications may face incorrect product selection.
Check the carton box label for the product description. The model number on the carton is 912080, and the actual product inside is 1.4mm devices, not 1.0mm.
Verify the carton box label matches the actual product inside. The label says 1.0mm, but the product is 1.4mm.
The carton box labels incorrectly state that the Juggerknot Mini Soft Anchors are 1.0mm products, but the actual items inside are 1.4mm devices.
The recall does not require immediate action; check the carton label to confirm the product type.
No specific injury risk is mentioned in the recall. The issue is a labeling mismatch, not a safety hazard.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2619-2025 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-2619-2025 from Biomet. 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.
