medical MODERATE Updated 2022-05-11

restor3d Inc. recalls Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N

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Recalled Product

Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument

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Hazard / Issue

Product labeled incorrectly. The lot was labeled with Small footprint when the product was Medium.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Model: 6110-N01-KTS01 Lot: 2022030005 UDI: 00840097504506

✅ 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 Non-Sterile Double Ended Trial →

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