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Cyclone Pocket BVM 1000

MICRO B.V.M. SYSTEMS LTD · Model PBVM KN · UDI-DI 07290016824070

BTM
10
510(k) clearances
1,897
Adverse events (164 deaths)
97
Recalls
74
Facilities

Description

"Pocket BVM is a manual emergency ventilator whose purpose is to manually apply positive pressure to a patient’s airways to support ventilation and oxygenation. The modified Pocket BVM incorporates bags and valve assemblies and is intended to provide emergency respiratory support to a patient through a tube inserted into the patient's airway or a face mask. The Pocket BVM device continues to maintain the functionality of existing devices and also has the advantage of small external dimensions (when packed) and light weight. It can be unpacked and made operational in seconds. "

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.