Class I recall due to failure or delay in delivery of therapy.
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LIFEPAK CR Plus Automated External Defibrillators (Physio-Control, Inc)
On September 16, 2009, In Food and Drug Administration, By admin
On September 12, 2009, In Food and Drug Administration, By admin
Nationwide recall due to risk of obstruction and inability to ventilate patient.
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Portex Uncuffed Pediatric-Sized Tracheal Tubes (sizes 2.5, 3.0 and 3.5 mm)
On September 9, 2009, In Food and Drug Administration, By admin
CONMED Corporation’s (Nasdaq: CNMD) CONMED Linvatec unit announced today a voluntary recall for certain model numbers of the PRO5 & PRO6 series battery handpieces manufactured prior to May 31, 2008, and certain lots of the MC5057 Universal Cable manufactured prior to December 1, 2006 used with certain of CONMED Linvatec’s electric powered handpieces.
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CONMED Corporation Announces Voluntary Recall of Certain Powered Surgical Instrument Products
On September 9, 2009, In Food and Drug Administration, By admin
Class 1 recall due to defect which may result in brain blood clot and blood vessel puncture.
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Penumbra Neuron 5F Select Catheter
On July 9, 2009, In Food and Drug Administration, By admin
Calico Cottage, Inc.
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Calico Cottage, Inc. Voluntarily Recalls 10 oz. Gourmet Hot Cocoa Mix Pouches Because Of The Possible Presence Of Salmonella