Philips heartstart pads recall
Webb5 feb. 2024 · Philips Pad Recall Philips M5071A (adult) and M5072A (infant/child) AED Pads A problem has been identified that could pose a risk for patients or users. HS1/OnSite/Home AED pads (PN: M5071A, M5072A) have been observed to experience gel separation from the foam/tin backing when peeled from the yellow plastic liner. WebbPhilips issued an Emergency Medical Device Correction regarding a potential gel peeling issue with the Adult SMART Pads Cartridge (M5071A) and the Infant/Child SMART Pads Cartridge (M5072A) for use specifically with the HeartStart HS1 AEDs (including …
Philips heartstart pads recall
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Webb9 feb. 2024 · Class 2 Device Recall Philips, HeartStart FR2 Defibrillator. Model M3860A affected serial numbers: A09G-04198 and 510800626 Model M3861A affected serial … Webb10 apr. 2024 · The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at...
WebbAny pad currently installed in or stored with an HS1/onsite/home aed could experience this problem, and it is not possible to know prior to patient use if your pad is affected because the pads are protected by a foil seal. Recall start date: Mar 2, 2024 Additional information Details Report a health or safety concern WebbPhilips is notifying customers of a potential issue with the Adult SMART Pads Cartridge (M5071A) and the Infant/Child SMART Pads Cartridge (M5072A) for use specifically …
WebbThe AED is both defective and a risk to health. Depending on what action must take place, a recall will be either a correction or a removal. A correction, or corrective action, is a recall that addresses the problem with the AED by correcting the issue in the place where the device is used or sold. Webb3 mars 2024 · Reason. Philips has become aware that a HeartStart HS1 Home, HS1 OnSite, FRx or FR2/FR2+ AED in customer's possession may have been omitted from one or more previous recalls or customer information notifications. Their records indicate that a potentially affected AED was shipped to a customer and the quantity affected, but the …
Webb4 feb. 2024 · Philips, REF M5071A, Adult. Smart PADS CARTRIDGE, 8+ years FOR USE WITH HEARSTART HS1 DEFIBRILLATORS: Code Information: ALL LOTS : Recalling Firm/ …
WebbPhilips will provide redesigned replacement SMART Pads to all end users when these are available. Philips has received 115 complaints since 2010 (of which 84 complaints were … portable carers shower screenWebbPhilips Healthcare Heartstart FRx AED with 2X Battery, 2X Pads, Infant Key, Case irrawaddy dolphin population geneticWebbField Safety Notice (579.0KB) Philips is notifying customers of a potential issue with the Adult SMART Pads Cartridge (M5071A) and the Infant/Child SMART Pads Cartridge (M5072A) for use specifically with the HeartStart HS1 AEDs. Philips has identified that for affected pads, some gel may fold onto itself, resulting in reduced surface area of ... portable car wash maltaWebb3 mars 2014 · If you are affected contact Philips immediately for a replacement device at 1-800-263-3342 and select OPTION 5. Live technical support is available Monday through Friday, 7:00AM to 5:00PM PST. You can also leave a message 24 hours a day, seven days a week and a customer support representative will return your call promptly on the next … portable carpet cleaner bethlehemWebbPads Recall - Landing Page Form URGENT MEDICAL DEVICE RESPONSE FORM PHILIPS HEALTHCARE This form consists of 4 pages. Please make sure to SUBMIT SURVEY on page 4. Reference: M5071A and M5072A Instructions: Please complete no later than 30 days from receipt. portable car wifi hotspotWebbThe Philips HeartStart FRx AED is the perfect AED for any scenario. Call us now for the best prices on Philips AEDs and Defibrillators 800-507-8244 Shipping Discount Cardiology ships via the Federal Express Service, which delivers shipments anywhere in the United States -- usually within 2-5 business days -- at low rates. portable car washing pumpWebb16 juli 2024 · Recall Number: Z-2427-2024: Recall Event ID: 88361: PMA Number: P160029 : Product Classification: Pads for Automated external defibrillators (non-wearable) - … irrawaddy magazine burmese version