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Resuscitators Recalled by Ventlab

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Taylor Jackson5 years ago

According to an FDA story, Ventlab Corporation initiated a nationwide recall of 14,602 of its manual resuscitators. The resuscitators may deliver little to no oxygen to the patient. This error might lead to hypoxia, hypoventilation, and other life-threatening injuries.

The recalled manual resuscitators were sold and distributed to hospitals, clinics and EMS units from March 2012 to July 2012.

What Was Recalled?

  • A complete list of recalled models can be found at
  • Product can be identified using a white label on the packaging bag, which includes the part number and lot number.

How to Handle Recalled Items

  • Anyone who has these manual resuscitators should stop using them and contact Ventlab for further instructions.
  • Anyone with questions may contact the company at 1-800-593-5654 or by e-mail at
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