HeartSine Technologies Ltd recall opens medical devices buyers to alternatives (2026-10-07)

HeartSine Technologies Ltd: recall opens medical devices buyers to alternatives (2026-10-07). Dated 29 days ago, it is in the active follow-up window. Score 25/100. 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 firmHeartSine Technologies Ltd
ProductHeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2
Replacement marketMedical devices
AgencyFDA medical devices
Severitystandard
HazardProducts were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check.
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-3270-2026
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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
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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 21:38:28 GMT

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Peer benchmark and outreach value: HeartSine Technologies Ltd 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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25 / 100 Switch Opportunity Score

    What is the RecallToCompetitorSwitch record for HeartSine Technologies Ltd?

    HeartSine Technologies Ltd recall (2026-10-07) in Medical devices: HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2

    How does HeartSine Technologies Ltd compare to other RecallToCompetitorSwitch records?

    It is 29 days old, still within a typical 45-day follow-up window. Its Switch Opportunity Score of 25/100 is modest; treat it as background rather than a priority.

    HeartSine Technologies Ltd vs. top 3 peers

    OrganizationLocationRecord date
    HeartSine Technologies Ltdfda2026-10-07
    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: Standard

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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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