Recall Z-1779-2008
Philips Medical Systems · initiated April 30, 2008
Product
Philips defibrillator, model M5066A. Sold in the US by Philips as an OTC under the brand name Philips "HeartStart On Site Defibrillator" and outside the U.S. by Philips with the brand name Philips "HeartStart Defibrillator". The HeartStart is an automated external defibrillator for use on site and consists of a computer with digital interface and cartridge containing pads.
Codes / lots: SN for Philips "HeartStart Defibrillator" and "HeartStart OnSite Defibrillator" : A05I-00001 A05I-00002 A05I-00003 A05I-00004 A05I-00005 A05I-00006 A05I-00007 A05I-00008 A05I-00009 A05I-00010 A05I-00012 A05I-00013 A05I-00014 A05I-00015 A05I-00016 A05I-00018 A05I-00019 A05I-00020 A05I-00021 A05I-00022 A05I-00023 A05I-00024 A05I-00025 A05I-00026 A05I-00027 A05I-00028 A05I-00029 A05I-00030 A05I-00031 A05I-00032 A05I-00033 A05I-00034 A05I-00035 A05I-00036 A05I-00037 A05I-00038 A05I-00039 A05I-00040 A05I-00041 A05I-00042 A05I-00043 A05I-00044 A05I-00045 A05I-00046 A05I-00047 A05I-00048 A05I-00049 A05I-00050 A05I-00052 A05I-00053 A05I-00054 A05I-00055 A05I-00056 A05I-00057 A05I-00058 A05I-00059 A05I-00060 A05I-00061 A05I-00062 A05I-00063 A05I-00064 A05I-00065 A05I-00066 A05I-00067 A05I-00068 A05I-00069 A05I-00070 A05I-00071 A05I-00072 A05I-00074 A05I-00075 A05I-00076 A05I-00077 A05I-00078 A05I-00079 A05I-00080 A05I-00081 A05I-00082 A05I-00083 A05I-00084 A05I-00085 A05I-00086 A05I-00087 A05I-00088 A05I-00089 A05I-00090 A05I-00092 A05I-00093 A05I-00094 A05I-00095 A05I-00096 A05I-00097 A05I-00098 A05I-00099 A05I-00100 A05I-00101 A05I-00102 A05I-00104 A05I-00105 A05I-00106 A05I-00107…
Reason for recall
Buttons Sticking - The On/Off and Shock buttons on the front panel of the device may stick in place when pressed and fail to respond to the button press, causing a delay in the delivery of a defibrillation shock when the system advises a shock.
FDA-determined cause: Component design/selection
Action taken
Three separate Urgent - Device Recall letter were sent out on April 30, 2008 via tractable letter using UPS. 1) The end-customer letter advises of the recall, contact information to arrange a replacement of the device and instructions for checking the equipment to insure it is working correctly. "If your HeartStart Home Defibrillator is one of the affected devices or if you have any questions about this recall, please contact Philips Healthcare at 1.800.263.3342, option 5, or visit www.HeartStartHome.com to arrange for a free replacement defibrillator. If you have given your HeartStart to someone else as a gift, please call us promptly and let us know how to contact that person to arrange for the replacement. While waiting for your replacement unit, Philips recommends that you perform a battery insertion test (BLT) of your HeartStart, as described in the Owner's Manual provided with it. Simply remove the battery, wait 5 seconds, reinstall the battery, then press the shock button when directed. After the BIT has finished, press the green On/Off button twice. If either button does not seem to work, please contact Philips immediate." 2) The dealer/distributor and retail letters advises of the recall; request that the dealer/distributor provide end-customer information. "As part of a coordinated effort involving notification of regulatory authorities, other Philips entities, and support personnel, Philips will be contacting all affected customers directly. It is not necessary for you or your sub-distributors to contact customers." 3) The international customer contacts will be made via established Philips sales and distribution channels. Philips will be replacing international units under a Field Change Order Process (to be provided by the firm). In addition, Philips will provide a website that will provide customers with information related to the recall (www.HeartStartHome).
Details
- Recall number
- Z-1779-2008
- Initiated
- April 30, 2008
- Posted by FDA
- July 9, 2008
- Terminated
- October 23, 2012
- Product code
- MKJ – Automated External Defibrillators (Non-Wearable)
- Quantity
- 3,959 units
- Distribution
- Worldwide including USA and countries of Austria, Australia, Canada, Colombia, German, Denmark, Dominican Republic, Spain, France, England, Ireland, Italy, Japan, Netherlands, Norway, New Zealand, Panama, Sweden, Singapore, and South Africa.
- Recalling firm
- Philips Medical Systems, Seattle, WA
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-1780-2008 | Laerdal "HeartStart Defibrillator", model M5067A, under Laerdal brand for Laerdal…Buttons Sticking - The On/Off and Shock buttons on the front panel of the device may stick in place when… | 04/30/2008Terminated |
| Z-1781-2008 | Philips "HeartStart Home" defibrillator, model M5068A and is sold in the US over the…Buttons Sticking - The On/Off and Shock buttons on the front panel of the device may stick in place when… | 04/30/2008Terminated |