medical HIGH RISK Updated 2023-05-24

Draeger Medical, Inc. recalls VentStar Basic (P)180, MP00351

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Recalled Product

VentStar Basic (P)180, MP00351

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Hazard / Issue

Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 04048675422068; All lots.

✅ 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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