Device Recall GOPump 의 리콜

Recall

65192

Class 1

Z-1452-2013

2013-05-10

2013-06-06

Terminated

United States

2014-03-07

USFDA

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=118194

Symbios medical products, indianapolis, indiana, is performing a voluntary recall of all gopumps found in the gopump rapid recovery system kits and all goblock kits manufactured with flow control components assembled prior to july 2012. the recall is being expanded after receiving additional reports relating to excessively high flow rates on the 150 ml reservoir, 2 ml/hr gopump (pn510031), and the.

Symbios sent UrgentMedical Device Recall notices to all consignees beginning May 10, 2013. A second corrected/amended notice was sent on May 14, 2013 to consignees and a National Press release was issued. May 30,2013, a third amended Urgent Recall Notice was sent to all consignees correcting the pump description and lot number range table on page 5 of the notice. The notices and press release provided identification of the recalled devices including devices in the previous February 2013 recall, described possible adverse events, and included directions to to quarantine product in a secure location, in preparation for return. Consignees were asked to call 317 225-4447 ext. 25, 8:00 a.m to 4:00 p.m. EDT to receive a Returned Goods Authorization Number prior to returning product. Consignees were asked to complete and return the Attached Verification Form. Question and Concerns should be addressed to 317-225-4447 ext 25.