The Recall Desk

Hazard

Motor Stall recalls

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

What the numbers show

Total
4
Critical
0
Severe
1
Most recent
2019-12-11

Of the 4 motor stall recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (25%) 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 motor stall 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.

1–4 of 4

  • HighFDA (Devices)·Z-0508-2020·2019-12-11

    Medtronic Synchromed II Pumps Recalled for Potential Motor Stall

    Medtronic is recalling Synchromed II programmable pumps due to a potential foreign particle that could cause a permanent motor stall.

    Product
    Synchromed II programmable pump, Model numbers 8637-20 and 8637-40
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0896-2018·2018-03-14

    Medtronic Recalls Unimplanted SynchroMed II Pumps Due to Motor Stall Risk

    Medtronic is recalling unimplanted SynchroMed II Model 8637 pumps to address a design flaw that can cause motor stalls due to corrosion.

    Product
    Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The implantable Model 8637 SynchroMed II programmable pump is part of an infusion system that stores and delivers a prescribed drug to a specific site. The implanted in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0497-2013·2012-12-19

    Medtronic SynchroMed II Pumps Recalled for Motor Stall Risk

    Medtronic is recalling SynchroMed II pumps because unapproved drugs can cause motor stalls and stop drug delivery.

    Product
    Medtronic SynchroMed II, Model 8637, (The SynchroMed¿ II Pump is supplied in 20 ml or 40 ml reservoir size.) Sterilized using ethylene oxide. The pump is part of an infusion system that stores and delivers a prescribed drug to a specific site. The implantable components of the Sy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2185-2012·2012-08-22

    CareFusion Recalls Alaris Pump Module 8100 Due to Motor Stalls

    CareFusion 303, Inc. is recalling Alaris Pump Module model 8100 units due to reports of motor stalls during infusion.

    Product
    Alaris Pump Module model 8100. Subsequent product code: FPA The Pump module is intended for facilities that utilize infusion for the delivery of fluids, medications, blood, and blood products using continuous or intermittent delivery through clinically acceptable routes of
    Category
    Medical Device
    Distribution
    Distributed nationwide