The Recall Desk

Hazard

Chemical Irritation recalls

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

What the numbers show

Total
11
Critical
0
Severe
1
Most recent
2024-06-25

Of the 11 chemical irritation 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 (9%) 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 chemical irritation 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.

1–11 of 11

  • HighCPSC·24281·2024-06-25

    MGA Entertainment Recalls Miniverse Make It Mini Sets with Liquid Resins

    MGA Entertainment recalls about 21 million Miniverse Make It Mini Sets with unused liquid resins due to risk of skin, eye, and respiratory irritation. The recalled sets contain acrylates in amounts prohibited in children's products.

    Product
    Miniverse Make It Mini Sets with Liquid Resins
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0598-2020·2019-12-11

    Allergan Recalls XEN Gel Stent Due to Residual Polishing Compounds

    Allergan is recalling XEN Gel Stent implants because residual polishing compounds on the injector needle may transfer to the patient's eye, causing irritation or inflammation.

    Product
    XEN Gel Stent, REF 5513-001(US Model), Sterile, RX Only, (01)10888628032439 ; Other Model Numbers: 5507-001(Global Model) and 5517-001(Australia model) Implant for glaucoma treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2444-2015·2015-09-02

    FDA Recalls Covidien Infant Heel Warmers Due to Breakage Risk

    The FDA is recalling 164,749 units of Covidien Infant Heel Warmers because they may break during activation, causing spillage and potential skin or eye irritation.

    Product
    Covidien Argyle Infant Heel Warmers (with tab) Item Code: MH00002T Product Usage: Intended for application of the right amount of heat to an infants heel for blood sampling.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1651-2014·2014-05-28

    Heraeus Kulzer Recalls Gluma Desensitizer Power Gel Due to Extrusion Risk

    Heraeus Kulzer is recalling Gluma Desensitizer Power Gel because it may extrude all at once, causing irritation, burning, or blistering to patients or dental professionals.

    Product
    Gluma Desensitizer Power Gel Product Usage: Usage: This is a class 2 medical device. For reduction or elimination of pain in exposed cervical areas that do not require restoration. It is also used for alleviation or reduction of dentinal sensitivity after preparation of teet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·14128·2014-03-06

    Canon Recalls PowerShot SX50 HS Cameras for Chemical Irritation Risk

    Canon is recalling about 14,000 PowerShot SX50 HS digital cameras because a chemical in the viewfinder rubber can cause skin or eye irritation. Consumers should stop using the cameras and contact Canon for a free repair.

    Product
    Canon PowerShot SX50 HS Digital Cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·11011·2010-10-15

    JAKKS Pacific Recalls Spa Factory Kits Due to Explosion and Projectile Hazards

    JAKKS Pacific is reannouncing a recall of Spa Factory Aromatherapy Fountain and Bath Benefits Kits because unvented jar caps can explode, causing injuries and property damage.

    Product
    Spa Factory™ Aromatherapy Fountain & Bath Benefits Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·05244·2005-08-17

    Almar Sales Recalls Water Watch Children's Watches Due to Ingestion Risk

    Almar Sales Co. is recalling about 50,400 Water Watch children's watches because the bands contain liquid petroleum distillates that can leak if punctured. One child reported mouth and throat irritation after ingesting the liquid.

    Product
    Water Watch
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·02518·2002-01-10

    Reed & Barton Recalls Powerscourt Sterling Teething Rings Due to Flux

    Reed & Barton is recalling Powerscourt Sterling Teething Rings because solder flux may irritate skin or mouths. No injuries have been reported.

    Product
    Powerscourt Sterling Teething Rings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·95019·1994-11-03

    CPSC Recalls FAB Color-Plus Laundry Detergent Due to High Sodium Hydroxide Levels

    Colgate-Palmolive is recalling approximately 25,000 containers of FAB liquid Color-Plus laundry detergent sold in specific regions due to high levels of sodium hydroxide that can cause skin irritation or injury.

    Product
    FAB liquid Color-Plus laundry detergent
    Category
    Consumer Product
    Distribution
    Distributed nationwide