The Recall Desk

Hazard

Missing Warning Label recalls

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

What the numbers show

Total
32
Critical
0
Severe
1
Most recent
2026-04-16

Of the 32 missing warning label 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 (3%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all missing warning label 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.

26–32 of 32

  • HighFDA (Devices)·Z-0215-2019·2018-10-31

    Siemens StreamLab Automation Modules Recalled for Missing Pacemaker Warning Label

    Siemens Healthcare Diagnostics is recalling 186 StreamLab Automation Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.

    Product
    STREAMLAB CORE UNIT / LYNX WITH IOM
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0216-2019·2018-10-31

    Siemens StreamLab Refrigerated Storage Module Recall for Missing Warning Label

    Siemens Healthcare Diagnostics is recalling StreamLab Refrigerated Storage Module 9000 units because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.

    Product
    STREAMLAB - REFRIGERATED STORAGE MODULE 9000
    Category
    Medical Device
    Distribution
    38 states
  • LowFDA (Devices)·Z-1909-2016·2016-06-08

    Affymetrix Recalls CytoScan Dx Assay Kits Due to Missing Warning Statements

    Affymetrix is recalling 507 CytoScan Dx Assay kits because FDA inspectors found that required warning statements were missing from product shipments.

    Product
    CytoScan¿ Dx Assay. The CytoScan Dx Assay consists of five reagent modules, wash buffers (WS), a microarray kit, and analysis software. The CytoScan Dx Assay consists of five reagent modules, wash buffers (WS), a microarray kit, and analysis software: MOD R LA, CytoScan¿ Dx P
    Category
    Medical Device
    Distribution
    15 states
  • HighCPSC·06071·2006-01-24

    L.L. Bean Recalls Safety Kits Due to Flashlight Magnet Interference

    L.L. Bean is recalling safety kits because the flashlight's magnet can disrupt compasses and implantable cardiac defibrillators.

    Product
    Auto Safety Kit, Auto Aid in a Bottle, Winter Safety Kit, and Outdoorsman in a Bottle
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·05552·2005-03-14

    Kawasaki Prairie 700 ATVs Recalled for Missing Age Warning Label

    Kawasaki is recalling about 1,140 Prairie 700 ATVs because they lack a required age recommendation warning label, posing a risk of serious injury to children under 16.

    Product
    Kawasaki Prairie™ 700 4x4 all-terrain vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide