The Recall Desk

Hazard

Laceration Risk recalls

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

What the numbers show

Total
5
Critical
0
Severe
1
Most recent
2025-05-21

Of the 5 laceration risk 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 (20%) 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 laceration 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.

1–5 of 5

  • HighFDA (Devices)·Z-1779-2025·2025-05-21

    Philips Intera 1.5T R11 MRI System Quadrature Body Coil Seal Adhesive Failure

    Philips is recalling Intera 1.5T R11 MRI systems because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could contact patients and cause skin injuries.

    Product
    Intera 1.5T R11, Model Number: 781170;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0930-2024·2024-02-14

    BrightView X Gamma Camera Detector May Fall, Causing Patient Injury

    Detectors in Philips BrightView X gamma cameras may fall unexpectedly due to component failure, risking patient injury including fractures and lacerations.

    Product
    BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 453560824741 453560829261;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0106-2024·2023-10-18

    Glass Vials in Laboratory Control Products Recalled for Breakage Risk

    Multichem P and related laboratory control products are recalled due to defective glass vials that may break during delivery or use, potentially exposing users to biohazardous material.

    Product
    Multichem P, Part Code 08P90-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·23776·2023-07-27

    Sky Wheels Play Component Recalled for Fall Hazard

    Soft Play is recalling about 3,500 Sky Wheels play components because the wheels can detach from the overhead rail, causing a fall hazard and risk of injury to children. The company has received 15 reports of detachment, including three reported injuries involving scalp lacerations.

    Product
    Sky Wheels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0328-2022·2021-12-22

    Kool-Aid Ice Blue Raspberry Lemonade Drink Mix Recalled for Glass and Metal

    Kraft Heinz Foods Company is recalling Kool-Aid ice blue raspberry lemonade drink mix powder (20 oz.) due to potential glass and metal contamination in the product.

    Product
    Kool-Aid ice blue raspberry lemonade drink mix powder 20 oz. UPC 043000954072
    Category
    Food
    Distribution
    Distributed nationwide