Resuscitators Recalled by Ventlab
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 http://www.fda.gov/Safety/Recalls/ucm324561.htm.
- 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 firstname.lastname@example.org.
Contact an Experienced Product Liability Attorney
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If you or a loved one have been injured by or have developed serious side-effects from the use of defective medications or pharmaceuticals, contact Thomas J. Henry immediately. We represent clients/victims all over the country. We are available 24/7, nights and weekends.