Percussionaire Corporation recall opens medical devices buyers to alternatives (2026-10-07)

Percussionaire Corporation: recall opens medical devices buyers to alternatives (2026-10-07). Dated 28 days ago, it is in the active follow-up window. Score 40/100. As of 2026-11-04, from CPSC, NHTSA and FDA device recalls (via our recall feeds), mapped to replacement markets.

Data as of · Compiled by Zalwin from CPSC, NHTSA and FDA device recalls (via our recall feeds), mapped to replacement markets

Free preview: all 9 published fields of this record are shown below. Locked: 320 related RecallToCompetitorSwitch records and the 5-column CSV export.

FieldValue
Recalling firmPercussionaire Corporation
ProductIn-Line Valve, Product Number: P5-TEE
Replacement marketMedical devices
AgencyFDA medical devices
Severitymedium
HazardLabeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anestheti
Recall date2026-10-07
Switch angleBuyers and retailers of the recalled medical devices need a compliant replacement; position your product on the specific hazard fixed, with documentation.
Original recall record/report/fdapulse/z-3320-2026
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  • Source agency: CPSC, NHTSA and FDA device recalls (via our recall feeds), mapped to replacement markets
  • Record date: 2026-10-07
  • Data refreshed: 2026-11-04
  • Refunds on request within 14 days

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Top RecallToCompetitorSwitch records (fda first): Boston Scientific Cork, Ltd. recall opens medical devices bu · Boston Scientific Cork, Ltd. recall opens medical devices bu · Boston Scientific Cork, Ltd. recall opens medical devices bu · Life Technologies Holdings Pte Ltd recall opens medical devi · Boston Scientific Cork, Ltd. recall opens medical devices bu · Browse all by state and category →

LIVE PUBLIC DATA Source: CPSC, NHTSA and FDA device recalls (via our recall feeds), mapped to replacement markets · Last refreshed: Wed, 04 Nov 2026 01:31:24 GMT

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Peer benchmark and outreach value: Percussionaire Corporation and 321 fda peers

  • fda RecallToCompetitorSwitch records like this one: 321
  • Timing: Medium: dated in the last 30 days
  • Estimated pipeline if you contact every fda peer: $64,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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40 / 100 Switch Opportunity Score

  • Medium severity.

What is the RecallToCompetitorSwitch record for Percussionaire Corporation?

Percussionaire Corporation recall (2026-10-07) in Medical devices: In-Line Valve, Product Number: P5-TEE

How does Percussionaire Corporation compare to other RecallToCompetitorSwitch records?

It is 28 days old, still within a typical 45-day follow-up window.

Percussionaire Corporation vs. top 3 peers

OrganizationLocationRecord date
Percussionaire Corporationfda2026-10-07
Ventec Life Systems, Inc.fda2026-10-28
Ventec Life Systems, Inc.fda2026-10-28
Ventec Life Systems, Inc.fda2026-10-28

Related records

RecallToCompetitorSwitch: Medical devices RecallToCompetitorSwitch: FDA medical devices RecallToCompetitorSwitch: Medium

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Built from official CPSC, NHTSA and FDA recall data; market mapping is our classification. Do not make claims about a competitor's recall beyond what the agency published, and follow advertising and comparative-claims rules. Not a consumer report and may not be used for FCRA purposes. Informational only; not legal, investment or procurement advice. Not affiliated with any agency or company listed.

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