The Recall Desk

Hazard

Safety Risk 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
1
Severe
0
Most recent
2018-06-20

Of the 4 safety risk recalls we have scored against our rubric, 1 (25%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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 safety risk 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-2139-2018·2018-06-20

    Ion Beam Applications Recalls Proteus ONE and Plus Devices

    Ion Beam Applications is recalling Proteus ONE and Proteus Plus medical devices because unauthorized modifications or third-party accessories may pose a safety risk.

    Product
    Proteus ONE and Proteus Plus
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Drugs)·D-600-2013·2013-06-19

    Olaax MAXILOSS Weight Advanced Recalled for Containing Unapproved Sibutramine

    Olaax International is recalling MAXILOSS Weight Advanced capsules because they contain sibutramine, an unapproved drug removed from the U.S. market for safety reasons.

    Product
    MAXILOSS Weight Advanced, 225 mg proprietary blend of herbs, supplied in 36 count capsules in Green & Blue Boxes, Formulated and distributed by Olaax Corp, Lakeland, FL
    Category
    Drug
    Distribution
    Distributed nationwide