Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0960-2025 — VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single Patient, 5pk -A51001, VDR4 Control Unit Tester -PRT 991, VDR W/SWIVEL T SINGLE PATIENT PHASITRON -PRT 992, VDR4 HUMIDIFICATION ADAPTER KIT, CASE OF 10 -PRT 993, VDR4 Humidifica

U.S. FDA — Device Enforcement · United States · 2024-12-23 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0960-2025
Date of alert: 2024-12-23
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Percussionaire Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00849436000259

Reported risk: Due to internal venturi component getting transiently stuck in the forward position within the breathing circuit and may cause a reduction of amplitude and volume of ventilation.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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