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Alaris Infusion Pumps

The FDA announced a Class I recall of Alaris Infusion Pumps on October 29, 2007.

Class I recalls are the most serious recalls, indicating that the product will most likely cause serious injury or death.
 
Alaris Infusion Pumps deliver medications and fluids to patients through intravenous, epidural, or intra-arterial methods. When the pumps were manufactured, the occluder springs were not assembled correctly, which can result in the patient receiving too much medication or fluid.
 
United States Marshals seized Signature Edition Gold pumps, model numbers 7130, 7131, 7230 and 7231 on August 25. Infusion pump model number 8100 is also defective. The seizure occurred after Alaris failed to follow the FDA’s medical device manufacturing regulations and failed to correct the violations after they were notified.
 
If you were injured by an Alaris pump, contact a personal injury attorney immediately. Injuries include over-infusion (receiving too much) medication into the bloodstream, which can cause injury and death.
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