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Mar 8, 2019 ... Identification number: RA-69224 Reason Affected products Affected Products IntraClude Intra-Aortic Occlusion Device Reason Edwards Lifesciences has received a limited number of customer reports regarding an interlumen leak between the cardioplegia lumen and pressure lumen in the device. If present, the leak will be detected after the device is advanced into the ascending
May 20, 2016 ...Black Diamond Recalls Black Diamond Brand Index Ascenders (left & right) Report a Concern Starting date: May 20, 2016 Posting date: May 20, 2016 Type of communication: Consumer Product Recall Subcategory: Sports/Fitness Source of recall: Health Canada Issue: Fall Hazard Audience: General Public Identification number: RA-58480 Affected products What you
May 18, 2018 ... be identified through normal monitoring of balloon pressure, and it causes the medical staff to continue adding inflation fluid to the balloon, typically about 2-5 ml every 10-15 minutes for up to 50 ml total, to maintain balloon pressure sufficient for adequate occlusion of the ascending aorta. Affected products IntraClude Intra-aortic Occlusion Device Lot or serial
Mar 30, 2012 ...
Mar 30, 2012 ... Black Diamond Recalls Black Diamond Brand Index Ascenders (left & right) Consumers should immediately stop using the product and contact Black Diamond to arrange for an inspection by Black Diamond or by place-of-purchase personnel, or directions for self-inspection. Black Diamond will replace any improperly manufactured units. For more information, consumers may
Jun 5, 2013 ... information regarding ZERIT® (stavudine, d4T). The following information will be incorporated into the Product Monograph: Reports have been received of rare occurrences of rapidly ascending neuromuscular weakness, mimicking the clinical presentation of Guillain-Barré syndrome (including respiratory failure), in HIV-infected patients receiving stavudine in combination