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AirLife

Carefusion Corporation · Model 2K7104 · UDI-DI 10885403220739

BTM Prescription
10
510(k) clearances
1,897
Adverse events (164 deaths)
97
Recalls
75
Facilities

Description

Pediatric Manual Resuscitator, 40"(1.0m) Oxygen ResevoirTubing, Pediatric Mask, Pressure Limiting Valve with Lock, 7' O2 tubing

Recalls

DateFirmReason
2026-05-08Datex-Ohmeda IncBlender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration se
2025-07-09Ambu Inc.Potential for the manometer port being blocked rendering the manometer non-functional.
2025-05-01SunMed Holdings, LLCAffected lots were manufactured with B/V Filter incorrectly attached to the wrong port (patient port instead of the exhalation port). If not noticed prior to patient use, there wou
2024-01-10Vyaire MedicalRisk of hypoventilation caused by duckbill and ring broken/disassembled, due to faulty mold/tooling producing out of specification components. Device failure may cause improper ven
2024-01-10Vyaire MedicalRisk of hypoventilation caused by duckbill and ring broken/disassembled, due to faulty mold/tooling producing out of specification components. Device failure may cause improper ven
2024-01-10Vyaire MedicalRisk of hypoventilation caused by duckbill and ring broken/disassembled, due to faulty mold/tooling producing out of specification components. Device failure may cause improper ven
2024-01-10Vyaire MedicalRisk of hypoventilation caused by duckbill and ring broken/disassembled, due to faulty mold/tooling producing out of specification components. Device failure may cause improper ven
2024-01-10Vyaire MedicalRisk of hypoventilation caused by duckbill and ring broken/disassembled, due to faulty mold/tooling producing out of specification components. Device failure may cause improper ven
2024-01-10Vyaire MedicalRisk of hypoventilation caused by duckbill and ring broken/disassembled, due to faulty mold/tooling producing out of specification components. Device failure may cause improper ven
2024-01-10Vyaire MedicalRisk of hypoventilation caused by duckbill and ring broken/disassembled, due to faulty mold/tooling producing out of specification components. Device failure may cause improper ven

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.