Product Alerts and Recalls
May 18, 2009
Philips Healthcare announced today that orders for the HeartStart FR2+ (M3860A and
M3861A) automated external defibrillators (AED) will no longer be accepted. After nine years on the market, the FR2+ is being discontinued.
Supplies, training accessories and technical support will still be available. Please click here to view the announcement. If you should have questions, please call your Southeastern Emergency Equipment sales representative or customer service person for more information and assistance.
April 13, 2009
Philips Healthcare has announced a voluntary recall affecting some of its HeartStart MRx Defibrillators/Monitors (model M3535A/M3536A). The voluntary action is due to a potential therapy switch failure that may cause spontaneous turn-on or failure to turn on. To date, there has been only one report of a suspected failure worldwide. This failure could not be confirmed and no patient impact was reported. Philips is taking this corrective action to proactively limit the possibility of this failure occurring in the future. The units affected are those that were manufactured by Philips from March 2006 to March 2009 with a serial number within the range of US00210406 and US00333123 plus a few additional units that had their therapy switches replaced within the relevant time period. Please click here to see the Field Safety Notice for more information regarding the potential problem, the serial numbers of the affected units, the actions that should be taken by end-users and the actions planned by Philips to correct the problem. Philips is currently in the process or contacting end-users regarding this potential problem. Southeastern Emergency Equipment is also sending letters and contacting all its affected customers.
September 23, 2008
CASMED 740 SERIES MONITOR - Product Correction Notification
The following serial numbers are the only units sold by Southeastern Emergency Equipment that are affected:
0815362
0815361
0812780
0810008
0809813
July 17, 2008
Important product notice from Informed regarding the EMS Field Guide - ALS version
May 14, 2008
Bedford Laboratories is voluntarily recalling Lot # 1156947 for Amiodarone Hydrochloride Injection, 150mg/3ml vials. Notification letters have been sent to all customers who purchased this product from Southeastern Emergency Equipment. If you have questions or need assistance with returning product, please contact our Customer Service Department by telephone at 1-800-334-6656 or via e-mail at customerservice@seequip.com.
Bedford Laboratories Amiodarone Recall Letter
