medical MODERATE Updated 2026-06-17

Medartis AG recalls Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-821

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Recalled Product

Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation

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Hazard / Issue

The cannulation of the CCS screw is not centered.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI/DI 07630037887706, Lot Numbers: 25444702, 24425542, 24404471, 25441997

✅ 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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