The Recall Desk

Hazard

Loss Of Therapy recalls

28 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
28
Critical
0
Severe
6
Most recent
2025-09-24

Of the 28 loss of therapy recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 6 (21%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all loss of therapy recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

26–28 of 28

  • HighFDA (Devices)·Z-1600-2016·2016-05-11

    Nuvectra Algovita Spinal Cord Stimulation Programmer Recall for Software Defect

    Nuvectra is recalling 17 Algovita Spinal Cord Stimulation System Clinical Programmers (Model 4500) because a software defect may prevent users from recharging the implantable pulse generator.

    Product
    Nuvectra, Algovita Spinal Cord Stimulation System Clinical Programmer, Model 4500. For use with Algovita Spinal Cord Stimulation Systems. The version of the software in the Clinician Programmer is v1.1.5. The Algovita Spinal Cord Stimulation system consists of a stimulator (
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0659-2016·2016-01-27

    Cyberonics Recalls VNS Therapy AspireSR Generators Due to Stimulation Failure

    Cyberonics is recalling 4,935 VNS Therapy AspireSR Generators worldwide after three reports of device resets that disabled stimulation output.

    Product
    VNS Therapy AspireSR Generator Model 106. Indicated for use as an adjunctive therapy in reducing the frequency of seizures.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1143-2014·2014-03-12

    Phillips Respironics Recalls Trilogy Ventilators Due to Power Board Defect

    Phillips Respironics is recalling 572 Trilogy ventilators worldwide because a defective power management board component may cause loss of therapy.

    Product
    Trilogy Ventilators The Respironics Trilogy 100 system provides continuous or intermittent ventilator support for the care of individuals who require mechanical ventilation. Trilogy 100 is intended for pediatric through adult patients weighing at least 5 kg (11 lbs.). The device
    Category
    Medical Device
    Distribution
    Distributed nationwide