The Recall Desk

Hazard

Unacceptable Variation 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
2018-11-14

Of the 2 unacceptable variation 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 unacceptable variation 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

  • ModerateFDA (Devices)·Z-0382-2019·2018-11-14

    Randox Recalls Liquid Cardiac Control CQ5053 Due to Unacceptable Variation

    Randox Laboratories is recalling Liquid Cardiac Control CQ5053 because the product is no longer suitable for controlling the Troponin T assay due to unacceptable variation between vials.

    Product
    Liquid Cardiac Control, CQ5053
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0381-2019·2018-11-14

    Randox Recalls Liquid Cardiac Control CQ5052 Due to Unacceptable Variation

    Randox Laboratories is recalling Liquid Cardiac Control CQ5052 because the product is no longer suitable for controlling the Troponin T assay due to unacceptable variation between vials.

    Product
    Liquid Cardiac Control, CQ5052
    Category
    Medical Device
    Distribution
    4 states