Philips heartstart pads recall

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August undefined, 2024

WebbPhilips FR2+ Heartstart Automatic External Defibrillator AED w/ Pads, No Battery. Condition: Used. “AED is used and was removed from a working environment. Physically … 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 …

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

WebbCall 800-263-3342 Maintaining the HeartStart HS1/OnSite/Home Pads and Battery Maintaining the HeartStart FRx Pads and Battery Have the reliability you need – on hand … 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, … darkly humorous

AED Pads Medical Device Recall Notice Philips

WebbPhilips 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 … WebbThe HS1 AED provides practically real-time guidance through step-by-step voice commands from pad placement to performing CPR. When every minute counts, Philips HeartStart HS1 AED is the partner by your side. Side by side. Step by step. Contact us Features Documentation Specifications Related products AED consumables and supplies WebbPhilips issued an Emergency Medical Device Notice regarding a potential gel peeling issue with the Adult SMART Pads Cartridge (M5071A) and the Infant/Child SMART Pads … darkly i gaze into the days ahead

AED recall Philips

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. 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. bishop high school ncWebb28 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 … darkly humorous horror toledo library blog

"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... " - Philips heartstart pads recall

Philips heartstart pads recall

AED Pads Medical Device Recall Notice Philips

Webb4 feb. 2024 · Philips, REF M5071A, Adult. Smart PADS CARTRIDGE, 8+ years FOR USE WITH HEARSTART HS1 DEFIBRILLATORS: Code Information: ALL LOTS : Recalling Firm/ … 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 …

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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. 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 …

Webb16 juli 2024 · Recall Number: Z-2427-2024: Recall Event ID: 88361: PMA Number: P160029 : Product Classification: Pads for Automated external defibrillators (non-wearable) - … 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.

Webb9 feb. 2024 · Class 2 Device Recall Philips, HeartStart FR2 Defibrillator. Model M3860A affected serial numbers: A09G-04198 and 510800626 Model M3861A affected serial … 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 ...

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

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. darkly i gaze into the days ahead meaningWebb9 feb. 2024 · Email to: [email protected] Or, Fax: 1 (833) 371-1011 2. A Philips representative will reach out to you to help you identify any affected AED. 3. After … bishop hill apartments stabbingWebb9 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 … bishop high school san diegoWebbTGA Recall Reference: RC-2024-RN-00538-1: Product Name/Description: Philips HeartStart HS1 Home, HS1 OnSite, FRx or FR2/FR2+ AED ARTG 92346 (Philips Electronics Australia Ltd Defibrillator - Non-rechargeable semi-automatic external defibrillator) Recall Action Level: Hospital: Recall Action Classification: Class I: Recall Action Commencement ... bishop hill antique agriculture associationWebbPhilips 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 … darkly humorous vignettes explorinWebbAny 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 bishop hillWebb25 jan. 2024 · This Philips Respironics December 2024 update is intended to provide healthcare providers, patients, and other stakeholders with updated information on the … darkly inclined