Philips Respironics, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1505-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.

Product Classification:

Class I

Date Initiated: March 19, 2024

Date Posted: April 24, 2024

Recall Number: Z-1505-2024

Event ID: 94263

Reason for Recall:

Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.

Status: Ongoing

Product Quantity: 9,999 units

Code Information:

Model No. DS2000X11B; UDI-DI: 606959052000; All units except those with software version 1.05.06.00.

Distribution Pattern:

Domestic: Nationwide Distribution; Foreign: AE, AR, AT, AU, BD, BE, BG, BO, BR, BS, CA, CH, CL, CN, CO, CZ, DE, DK, DZ, EC, EE, EG, ES, FI, FR, GB, GE, GF, GI, GR, GT, HK, HR, HU, ID, IE, IL, IN, IT, JE, JO, JP, KE, KR, KW, LB, LT, MA, ME, MK, MM, MQ, MT, MX, MY, NG, NL, NO, NP, NZ, OM, PA, PE, PF, PH, PK, PL, PR, PT, PY, QA, RE, RO, RS, RU, SA, SE, SG, SI, SK, TH, TN, TR, TW, UA, US, UY, VN, YT, ZA, ZW.

Voluntary or Mandated:

Voluntary: Firm initiated