Philips heartstart pads recall

Author: luwh

August undefined, 2024

WebbThe recall affects only the Philips HeartStart OnSite, HS1, FRx and Home Defibrillator AEDs; The Philips HeartStart FR, Forerunner, FR2 and FR2+ AEDs are not affected, but these devices are old and should be replaced with newer life-saving devices like the OnSite model; Only AEDs manufactured from 2002 to early 2013 are affected by the ... 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 …

M5071A - Philips Heartstart Adult Smart Pads

WebbThe 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. WebbField 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 ... nj change of license form

AED recall Philips Healthcare

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. Webb25 jan. 2024 · This Philips Respironics December 2024 update is intended to provide healthcare providers, patients, and other stakeholders with updated information on the … nj child neglect statute

Class 2 Device Recall Philips, HEARTSTART, INFANT/CHILD …

Philips Pad Recall - Action First Aid

WebbPads 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. WebbPhilips Healthcare Heartstart FRx AED with 2X Battery, 2X Pads, Infant Key, Case nursing home business plansWebbThe Philips HeartStart FRx defibrillator features intuitive, step-by-step voice instructions, including CPR guidance, and an audible metronome to help guide basic life support … nursing home business

"WebbRecall Status 1: Terminated 3 on April 29, 2024: Recall Number: Z-2549-2024: Recall Event ID: 83681: 510(K)Number: K020715 Product Classification: Automated external … " - Philips heartstart pads recall

Philips heartstart pads recall

Class 2 Device Recall Philips, HeartStart FR2 Defibrillator

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 … WebbThe Philips HeartStart Home Defibrillator is the first and only defibrillator available without a prescription. Designed with you in mind, HeartStart Home is easy to set up and …

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WebbPhilips is offering trade-in rebates depending on the age and model of the affected AED. To request a warranty exchange unit or a trade-in rebate, or to obtain additional information, contact your local Philips representative. In the United States, contact Philips directly at 1-800-263-3342. Q: Are the AEDs under this recall safe to use? A: Yes. Webb9 feb. 2024 · Class 2 Device Recall Philips, HeartStart FR2 Defibrillator. Model M3860A affected serial numbers: A09G-04198 and 510800626 Model M3861A affected serial numbers: A09H-00436 and A07J-03514. Customers were not notified of previous recalls associated with various defibrillator models. On February 11, 2024, Philips issued a …

WebbPhilips is offering trade-in rebates depending on the age and model of the affected AED. To request a warranty exchange unit or a trade-in rebate, or to obtain additional information, contact your local Philips representative. In the United States, contact Philips directly at 1-800-263-3342. Q: Are the AEDs under this recall safe to use? A: Yes. Webb4 feb. 2024 · Philips, REF M5071A, Adult. Smart PADS CARTRIDGE, 8+ years FOR USE WITH HEARSTART HS1 DEFIBRILLATORS: Code Information: ALL LOTS : Recalling Firm/ …

Webb14 mars 2024 · Recalling Firm/ Manufacturer: Philips Electronics North America Corp. 22100 Bothell Everett Hwy Bothell WA 98021-8431: For Additional Information Contact: … Webb3 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 …

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

Webb28 juli 2024 · A problem has been identified in certain philips m5072a heartstart infant/child smart pads cartridges (lot y111220-01) which are used with the philips … nursing home buying programsWebbPhilips HeartStart OnSite Adult Smart Pads have specific weight and age guidelines: OnSite Adult SMART Pads can be used for adults and children who are 8 years old and older, and/or 55 pounds and over. There is a 2 … nursing home business plan pdfWebb16 juli 2024 · Recall Number: Z-2427-2024: Recall Event ID: 88361: PMA Number: P160029 : Product Classification: Pads for Automated external defibrillators (non-wearable) - … nursing home business planWebb12 jan. 2024 · 12 January 2024. On 10 January 2024, Philips expanded their Product Defection Correction for the HeartStart AEDs. Due to customer feedback and complaints, Philips is notifying additional customers who may have received affected HeartStart AED machines who were not aware of the initial notification. Philips has advised that … nj check business registrationWebbThe recall is being initiated due to incorrect age range labeling (8+ yrs) on the foil packaging for infant/child pad cartridges. The infant/child pad cartridge is designed for use with the defibrillator An Infant/Child pad cartridge should not be used on an adult because it delivers lower energy (50 J vs 150 J) than the Adult pads cartridge and may therefore … nursing home business for saleWebb9 feb. 2024 · Class 2 Device Recall Philips, HeartStart FR2 Defibrillator. Model M3860A affected serial numbers: A09G-04198 and 510800626 Model M3861A affected serial … nursing home butler alabamaWebbPhilips is offering trade-in rebates depending on the age and model of the affected AED. To request a warranty exchange unit or a trade-in rebate, or to obtain additional information, … nursing home butler pa