The Recall Desk

Hazard

Medication Discontinuation recalls

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

What the numbers show

Total
2
Critical
0
Severe
0
Most recent
2019-06-12

Of the 2 medication discontinuation recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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 medication discontinuation 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.

1–2 of 2

  • HighFDA (Devices)·Z-1715-2019·2019-06-12

    Flowonix Prometra II Pump Recall for Unexpected Shutdowns

    Flowonix Medical Inc is recalling 6,445 Prometra II Programmable Pumps because a software defect can cause the device to shut down unexpectedly.

    Product
    Prometra II Programmable Pump, Cat. No. 13827 For intrathecal infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1716-2019·2019-06-12

    Flowonix Prometra II Pump Recall for Unexpected Shutdowns

    Flowonix Medical Inc. is recalling 163 Prometra II Programmable Pumps due to a software defect that can cause unexpected shutdowns.

    Product
    Prometra II Programmable Pump (Clinical), Cat. No. 01827 For intrathecal infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide