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Field Safety Notice Philips Respironics Sleep and Respiratory Care (ICN 1819)

Important Customer Notice Update

Ref: 2022/1819 ICN Number: 1819
  • This ICN is being updated following receipt of the Field Safety Notice dated 8 December 2022, from Philips regarding updating the existing ‘Contraindications’ and ‘Warnings’ for:
    • Amara View Minimal Contact Full-Face Mask
    • DreamWear Full Face Mask
    • DreamWisp Nasal Mask with Over the Nose Cushion
    • Wisp Nasal Masks, Wisp Youth Nasal Masks
    • Therapy Mask 3100 NC/SP.
  • There are 64 product codes affected.
  • See our Downloads section to access the product listing for further information on the affected product codes and Field Safety Notice for information on products affected.

MHRA: 2022/008/015/596/001
NHS Supply Chain Reference: 48

Alert:

  • Philips Respironics has issued a Field Safety Notice for five products:
    • Amara View Minimal Contact Full-Face Mask
    • DreamWear Full Face Mask
    • DreamWisp Nasal Mask with Over the Nose Cushion
    • Wisp Nasal Masks and Wisp Youth Nasal Masks
    • Therapy Mask 3100 NC/SP.
  • The supplier is updating its existing ‘Contraindications’ and ‘Warnings’.
  • Use of the mask is contraindicated for patients and their household members, caregivers and bed partners that may be in close vicinity to patients using the masks that have implanted devices that may be affected by magnets.
  • Magnets with a magnetic field strength of 400 mT are used in the mask, with the exception of the devices identified in the contraindication.
  • Please ensure the mask is kept at least 6 inches (approx. 15.24 cm) away from any other medical implants or medical devices that can be impacted by the magnetic fields to avoid possible effects from localized magnetic fields. This includes household members, caregivers, and bed partners that may be in close vicinity to patients that use the masks.

Products Affected:

  • There are 36 products are affected.
  • See our Downloads section to access the product listing and Field Safety Notice for further information on the affected product codes.

Next Steps:

  • Read and follow the full instructions in the Field Safety Notice and share with all users of the affected products.
  • Identify patients who have an implanted device where use of the magnetic mask is contraindicated and follow steps outlined in the Field Safety Notice.
  • We will provide copies of the patient version of the Field Safety Notice and FAQs document to all patients using the affected devices.
  • We will update this ICN with details of alternative products after clinical guidance has been completed.
  • If you need any further information or support concerning this issue, please contact your local Philips Respironics representative: UK Philips Customer Care Service Centre on 0870 532 9741.
  • If you have any further questions, please contact your local NHS Supply Chain Customer Relationship Manager or Customer Service Advisor.

Downloads ▼

  • 1819 Philips Field Safety Notice 12 January 2023

    A PDF detailing the Field Safety Notice for ICN 1819.
  • 1819 Philips Field Safety Notice for Patients 26 September 2022

    A PDF detailing the Field Safety Notice for Patients for ICN 1819.
  • 1819 Philips Frequently Asked Questions 26 September 2022

    A PDF detailing the FAQs for ICN 1819.
  • 1819 Philips Product Listing 12 January 2023

    An Excel file showing the product listing for ICN 1819.