medical MODERATE Updated 2017-05-24

Biomet Microfixation, LLC recalls Biomet Microfixation TraumaOne System Surgical Tray - Model

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Recalled Product

Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600

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Hazard / Issue

Part of the number on the tray lid differ from the part number on the base.

Issued by

FDA

Affected States: AL, MO, UT
Lot/Code Info: Part Number 46-1610 // Lot Number 709730 Part Number 46-1610 // Lot Number 709740 Part Number 46-1620 // Lot Number 709710 Part Number 46-1620 // Lot Number 709720

✅ 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.

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Search Amazon for Biomet Microfixation TraumaOne System →

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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