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Latest Class I recall Stories

2014-09-09 23:01:17

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,

2014-08-14 23:01:16

The Firm is representing numerous individuals who allegedly suffered life-threatening cardiovascular injuries prior to the 2012 NaturaLyte and GranuFlo recall. New

2014-07-03 16:23:13

GREENSBORO, N.C., July 3, 2014 /PRNewswire/ -- ConvaTec has announced that the U.S.

2014-06-18 23:08:45

Bellwether Trials Expected to Begin in Either Mid-2015 or Early 2016 DALLAS (PRWEB) June 18, 2014 The national law firm of

2014-06-16 23:12:21

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.

2014-06-10 23:16:23

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.

2014-06-03 23:02:32

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.

2014-05-30 23:16:50

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.

2014-05-29 23:15:44

On May 22, the FDA announced that Baxter Abacus TPN Calculation Software is recalled (Class I) because software errors may cause toxic/overdose symptoms.

2014-05-28 23:16:04

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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