• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall HeartStart defibrillator

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards | Inspections
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
 Class 2 Recall
HeartStart defibrillator
see related information
Date Posted July 09, 2008
Recall Status1 Open
Recall Number Z-1781-2008
Recall Event ID 47833
Premarket Notification
510(K) Numbers
K020715  K040904 
Product Classification Over-The-Counter Automated External Defibrillator - Product Code NSA
Product Philips "HeartStart Home" defibrillator, model M5068A and is sold in the US over the counter. The HeartStart is an automated external defibrillator for use on site and consists of a computer with digital interface and cartridge containing pads.
Code Information SN for Philips "HeartStart Home": A05I-00017, A05I-00403, A05I-00412, A05I-00413, A05I-00414, A05I-00415, A05I-00417, A05I-00418, A05I-00419, A05I-00420, A05I-00421, A05I-00423, A05I-00424, A05I-00425, A05I-00426, A05I-00428, A05I-00429, A05I-00430, A05I-00431, A05I-00433, A05I-00434, A05I-00435, A05I-00436, A05I-00437, A05I-00438, A05I-00439, A05I-00440, A05I-00441, A05I-00442, A05I-00443, A05I-00444, A05I-00445, A05I-00446, A05I-00447, A05I-00448, A05I-00449, A05I-00450, A05I-00476, A05I-00496, A05I-00501, A05I-00503, A05I-00504, A05I-00505, A05I-00506, A05I-00509, A05I-00511, A05I-00512, A05I-00513, A05I-00515, A05I-00520, A05I-00528, A05I-00529, A05I-00530, A05I-00531, A05I-00535, A05I-00537, A05I-00539, A05I-00540, A05I-00541, A05I-00542, A05I-00544, A05I-00545, A05I-00549, A05I-00604, A05I-00605, A05I-00607, A05I-00609, A05I-00610, A05I-00612, A05I-00613, A05I-00614, A05I-00656, A05I-00665, A05I-00666, A05I-00667, A05I-00668, A05I-00669, A05I-00670, A05I-00671, A05I-00672, A05I-00673, A05I-00674, A05I-00676, A05I-00677, A05I-00678, A05I-00679, A05I-00680, A05I-00681, A05I-00682, A05I-00683, A05I-00684, A05I-00685, A05I-00686, A05I-00687, A05I-00688, A05I-00689, A05I-00690, A05I-00691, A05I-00692, A05I-00693, A05I-00694, A05I-00695, A05I-00697, A05I-00698, A05I-00699, A05I-00700, A05I-00747, A05I-00749, A05I-00750, A05I-00751, A05I-00752, A05I-00753, A05I-00754, A05I-00755, A05I-00756, A05I-00757, A05I-00758, A05I-00759, A05I-00760, A05I-00761, A05I-00762, A05I-00764, A05I-00771, A05I-00772, A05I-00776, A05I-00777, A05I-00778, A05I-00779, A05I-00780, A05I-00785, A05I-00808, A05I-00810, A05I-00813, A05I-00814, A05I-00815, A05I-00817, A05I-00818, A05I-00819, A05I-00820, A05I-00821, A05I-00822, A05I-00823, A05I-00824, A05I-00828, A05I-00830, A05I-00832, A05I-00833, A05I-00837, A05I-00841, A05I-00842, A05I-00843, A05I-00844, A05I-00845, A05I-00846, A05I-00848, A05I-00849, A05I-00850, A05I-00868, A05I-00871, A05I-00874, A05I-00877, A05I-00878, A05I-00882, A05I-00883, A05I-00884, A05I-00885, A05I-00886, A05I-00887, A05I-00888, A05I-00889, A05I-00890, A05I-00891, A05I-00892, A05I-00893, A05I-00894, A05I-00895, A05I-00896, A05I-00897, A05I-00898, A05I-00899, A05I-00900, A05I-00901, A05I-00902, A05I-00903, A05I-00904, A05I-00905, A05I-00906, A05I-00907, A05I-00909, A05I-00910, A05I-00911, A05I-00912, A05I-00913, A05I-00914, A05I-00915, A05I-00916, A05I-00917, A05I-00918, A05I-00920, A05I-00921, A05I-00922, A05I-00923, A05I-00942, A05I-01010, A05I-01195, A05I-01257, A05I-01267, A05I-01288, A05I-01289, A05I-01290, A05I-01292, A05I-01293, A05I-01295, A05I-01296, A05I-01298, A05I-01299, A05I-01357, A05I-01380, A05I-01381, A05I-01397, A05I-01399, A05I-01444, A05I-01450, A05I-01487, A05I-01494, A05I-01501, A05I-01502, A05I-01503, A05I-01506, A05I-01507, A05I-01513, A05I-01517, A05I-01520, A05I-01521, A05I-01522, A05I-01524, A05I-01525, A05I-01547, A05I-01549, A05I-01568, A05I-01576, A05I-01579, A05I-01582, A05I-01584, A05I-01587, A05I-01591, A05I-01602, A05I-01606, A05I-01607, A05I-01608, A05I-01609, A05I-01610, A05I-01611, A05I-01612, A05I-01613, A05I-01614, A05I-01615, A05I-01616, A05I-01626, A05I-01635, A05I-01636, A05I-01637, A05I-01653, A05I-01656, A05I-01664, A05I-01665, A05I-01667, A05I-01670, A05I-01671, A05I-01680, A05I-01684, A05I-01685, A05I-01686, A05I-01715, A05I-01718, A05I-01720, A05I-01722, A05I-01723, A05I-01731, A05I-01732, A05I-01734, A05I-01740, A05I-01751, A05I-01798, A05I-01799, A05I-01800, A05I-01851, A05I-01852, A05I-01853, A05I-01858, A05I-01859, A05I-01860, A05I-01861, A05I-01862, A05I-01864, A05I-01865, A05I-01866, A05I-01867, A05I-01868, A05I-01872, A05I-01873, A05I-01876, A05I-01877, A05I-01919, A05I-01920, A05I-01922, A05I-01924, A05I-01926, A05I-01941, A05I-01943, A05I-01953, A05I-01956, A05I-01957, A05I-01958, A05I-01959, A05I-01960, A05I-01961, A05I-01963, A05I-01964, A05I-01965, A05I-01966, A05I-01968, A05I-01971, A05I-01972, A05I-02019, A05I-02158, A05I-02232, A05I-02247, A05I-02272, A05I-02274, A05I-02277, A05I-02278, A05I-02279, A05I-02281, A05I-02287, A05I-02292, A05I-02314, A05I-02718, A05I-02833, A05I-02840, A05I-02850, A05I-02851, A05I-02856, A05I-02873, A05I-02877, A05I-02960, A05I-02961, A05I-02985, A05I-02993, A05I-03011, A05I-03032, A05I-03053, A05I-03069, A05I-03098, A05I-03099, A05I-03101, A05I-03114, A05I-03117, A05I-03123, A05I-03205, A05I-03215, A05I-03216, A05I-03217, A05I-03357, A05I-03472, A05I-03473, A05I-03523, A05I-03524, A05I-03525, A05I-03561, A05I-03563, A05I-03566, A05I-03572, A05I-03584, A05I-03599, A05I-03601, A05I-03774, A05I-03775, A05I-03776, A05I-03777, A05I-03784, A05I-03798, A05I-03851, A05I-04019, A05I-04136, A05I-04290, A05I-04765, A05I-04769, A05I-04771
Recalling Firm/
Manufacturer
Philips Medical Systems
2301 5th Ave Ste 200
Seattle, Washington 98121
For Additional Information Contact Dennis Daniels
206-664-5000
Manufacturer 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 2
DESIGN: Component Design/Selection
Action 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).
Quantity in Commerce 389 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.
Total Product Life Cycle TPLC Device Report

 
1 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
510(K) Database 510(K)s with Product Code = NSA and Original Applicant = PHILIPS MEDICAL SYSTEMS
-
-