Biomet Juggerknot Mini Soft Anchors Recall: Wrong Product in Box
Biomet recalls Juggerknot Mini Soft Anchors (model 912080) due to incorrect product labels in shipping cartons. This mismatch may cause confusion for users.
Lower-risk recall
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.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/51371-biomet-juggerknot-mini-soft-anchors-recall-wrong-product-in-box.
Source Summary by GovInfoNow · govinfonow.com/recall/51371-biomet-juggerknot-mini-soft-anchors-recall-wrong-product-in-box · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2619-2025
Cite this page
“Biomet Juggerknot Mini Soft Anchors Recall: Wrong Product in Box.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51371-biomet-juggerknot-mini-soft-anchors-recall-wrong-product-in-box. Based on FDA recall #Z-2619-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2619-2025%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Biomet- Category
Medical device
What to do — step by step
Check Product Label
Verify the carton box label matches the actual product inside. The label says 1.0mm, but the product is 1.4mm.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 22 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if I have this product?
The recall does not require immediate action; check the carton label to confirm the product type.
Is there a risk of injury from this product?
No specific injury risk is mentioned in the recall. The issue is a labeling mismatch, not a safety hazard.
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Where this comes from
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.
- Official source: FDA Recall #Z-2619-2025 (September 9, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2619-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.