The Recall Desk

Hazard

Bruising recalls

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

What the numbers show

Total
9
Critical
0
Severe
1
Most recent
2022-05-18

Of the 9 bruising 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 (11%) 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 bruising 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.

1–9 of 9

  • HighFDA (Devices)·Z-1041-2022·2022-05-18

    Philips Hemodynamic Application fails to set neonatal blood pressure mode

    The Philips Hemodynamic Application, Model 722463, may not automatically switch to neonatal mode for blood pressure monitoring, potentially applying excessive cuff pressure that could cause bruising, nerve damage, or bone deformity in newborns.

    Product
    Philips Hemodynamic Application, Model Number 722463, Software Version Number: R1.2.2 and R1.2.3. For visualization and analysis of patient hemodynamic data in the Philips Interventional Hemodynamic System.
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0363-2014·2013-11-27

    Stryker Rose Bed Siderail Latch Failure Recall

    Stryker is recalling Model FL14E Rose Beds because siderails may appear latched when they are not, posing a risk of patient injury.

    Product
    Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable long-term care bed intended for medical purposes that consists of a bed with a built-in motor and controls that can be operated to adjust the height and surface contour of the bed. The device includes movable and lat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·10343·2010-09-14

    Coleman Recalls Water-Activated Spotlights Due to Risk of Impact Injury

    The Coleman Company is recalling WaterBeam 4D water-activated spotlights because the lens assembly can detach, posing a risk of impact injuries.

    Product
    Coleman® WaterBeam™ 4D Water-Activated Floating Spotlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·07238·2007-07-17

    Genuine Innovations Recalls Combination Tire Inflators and Hand Pumps

    Genuine Innovations is recalling about 55,000 combination tire inflators and hand pumps because they can shatter under pressure, posing risks of lacerations and bruising.

    Product
    Combination Tire Inflator and Hand Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·05600·2005-09-02

    Aqua Scout Recalls Water Scooters Due to Battery Ejection Risk

    Aqua Scout is recalling water scooters because hydrogen gas buildup can force the battery cover to eject, posing an injury risk.

    Product
    Aqua Scout Water Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·99128·1999-06-24

    Evenflo Snugli Soft Infant Carriers Recalled Due to Fall Risk

    Evenflo and Hufco-Delaware are recalling 327,000 Snugli soft infant carriers because small infants can slip through leg openings and fall.

    Product
    Soft Infant Carriers Recalled by Evenflo & Hufco-Delaware
    Category
    Consumer Product
    Distribution
    Distributed nationwide