Latest Class I recall Stories
A Class I recall designation by the FDA indicates that use of the recalled medical device may potentially lead to serious adverse reactions or death. Port Washington,
The Firm is representing numerous individuals who allegedly suffered life-threatening cardiovascular injuries prior to the 2012 NaturaLyte and GranuFlo recall. New
GREENSBORO, N.C., July 3, 2014 /PRNewswire/ -- ConvaTec has announced that the U.S.
Bellwether Trials Expected to Begin in Either Mid-2015 or Early 2016 DALLAS (PRWEB) June 18, 2014 The national law firm of
On June 13, the FDA notified of a recall (Class I) of Smiths Medical Portex Low Dead Space Connector with Sideport, 3.5mm because one lot was mislabeled.
On May 2, the FDA announced that Abbott Acclaim and Hospira Acclaim Encore Infusion Pumps, by Hospira, are recalled (Class I) due to broken door assemblies.
The Firm is representing numerous clients in GranuFlo Lawsuits, all of which allege the use of GranuFlo or NaturaLyte dialysis concentrates caused serious, and sometimes deadly, heart injuries.
On May 23, the FDA announced that Fisher and Paykel Healthcare Infant Nasal CPAP Prongs are recalled because prongs may detach from nasal tubing and interrupt therapy.
On May 22, the FDA announced that Baxter Abacus TPN Calculation Software is recalled (Class I) because software errors may cause toxic/overdose symptoms.
On May 12, the FDA announced that Maquet Datascope Intra-Aortic Balloon Pumps are recalled due to failure of a fan assembly.
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