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Recall Observatory FDA recall evidence

Device product

Philips OmniLab Advanced + with Heated Tube Humidifier, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.

Z-1659-2022

August 26, 2022

Class I

Product summary

Firm
Philips Respironics, Inc.
Event
Event 90695
Status
Ongoing
Classification
Class I
Quantity
8 units
Official record key
device-enforcement:Z-1659-2022

Official wording

Reason: Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.

Code information: UDI-DI: 606959067837, 606959068001; Model No.: 1111124, R1111124; Serial No. L29084645477C, L303986771E8D, L303987043BC2, L3039871356A5, L30398768A57E, L303987892EE7, L30398795FD53, L30398849CD80

Distribution pattern: Domestic: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NV, NY, OH, OK, OR, PA, TN, TX, VA, VT, WA, WI, WV, & WY. Foreign: Australia, Austria, Bangladesh, Brazil, Canada, China, Denmark, Egypt, France, Germany, Hong Kong, Hungary, India, Israel, Italy, Japan, Malaysia, Mexico, Myanmar, Philippines, Qatar, Serbia, Singapore, Taiwan, Thailand, Turkey, UAE, & UK.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.