medical MODERATE Updated 2025-10-01

Biomet, Inc. recalls Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080

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Recalled Product

Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 00880304520950; Lot Number 0002713620

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Juggerknot Mini Soft Anchors, →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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