The Recall Desk

Hazard

Skin Irritation recalls

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

What the numbers show

Total
76
Critical
0
Severe
4
Most recent
2026-08-12

Of the 76 skin 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 4 (5%) 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 skin 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.

1–25 of 76

  • HighFDA (Devices)·Z-2670-2026·2026-07-08

    Radius VSM ECG Pre-connected Set Recalled for Incorrect Heart Rate Detection

    Masimo Corporation is recalling Radius VSM ECG pre-connected sets because the ECG electrode assembly may incorrectly detect extreme bradycardia or tachycardia and trigger false alarms on patients with normal heart rates, potentially distracting clinicians from true positive alarms and delaying treatment.

    Product
    Radius VSM ECG pre-connected Set, REF: 4842, 4695
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2671-2026·2026-07-08

    Radius VSM Disposable NIBP Cuff recalled for rough edges

    Masimo Corporation is recalling Radius VSM Disposable NIBP Cuffs (blood pressure cuffs) with lot numbers 21G6S through 25ADF because they may contain rough edges that could cause skin irritation or redness.

    Product
    Radius VSM Disposable NIBP Cuff, REF: 4825, 4826
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·26526·2026-06-04

    Children's Tiny Land Play Tents Recalled for Skin and Eye Irritation Risk

    Tiny Land Inc. is recalling about 7,500 children's play tents because fiberglass poles can shed fibers, causing skin and eye irritation. Consumers should stop using the tents immediately and contact Tiny Land for a free repair kit with plastic replacement poles.

    Product
    Children's Tiny Land Play Tents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·26057·2025-10-30

    Glow stick bracelets recalled because green bracelet can leak and irritate

    About 6,600 Destination Holiday Glow Light Stick bracelet 12-packs are being recalled because the green bracelet can leak, posing a skin irritation hazard.

    Product
    Destination Holiday Glow Light Stick Bracelets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25197·2025-03-27

    Cra-Z-Art Gemex and Gel2Gem Jewelry Kits Recalled for Chemical Irritation Risk

    LaRose Industries is recalling about 224,100 Cra-Z-Art Gemex and Gel2Gem jewelry kits because the resin liquid can cause skin, eye, and respiratory irritation in children when inhaled, touched, or ingested.

    Product
    Cra-Z-Art Gemex/Gel2Gem Jewelry Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0797-2025·2025-01-08

    3M Unitek Orthodontic Primer Recalled Due to Bond Failures and Skin Irritation

    3M Unitek is recalling Transbond Plus Self-Etching Primer used in orthodontic bonding due to reports of bracket bond failures and skin irritation or blistering.

    Product
    3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self Etching Primer is an orthodontic all-in-one etchant and primer that is used in the bonding process of orthodontic appliances to teeth.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·24337·2024-08-08

    Finger-Ease Guitar String Lubricants Recalled Due to Skin Irritation Risk

    Chem-Pak is recalling Finger-Ease Guitar String Lubricants because one production batch contains a contaminant that poses a risk of skin irritation. One report of minor skin irritation has been received.

    Product
    Finger-Ease Guitar String Lubricants
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2320-2024·2024-07-17

    Medical examination gloves recalled for skin irritation and disintegration

    SVS LLC is recalling 155,540 boxes of non-sterile nitrile examination gloves due to reported skin irritation, glove disintegration with certain cleaning solutions, and size mislabeling. Gloves were distributed nationwide across eight U.S. states.

    Product
    Non-sterile, single use, disposable gloves intended for medical purposes to be worn on the hands of examiners to prevent contamination between a patient and an examiner. The gloves are nitrile, powder-free, ambidextrous, and blue-colored with a beaded cuff. The range of sizes inc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1615-2024·2024-05-01

    LightStrike Blackout Curtains Recalled Due to Inadequate UV and Ozone Protection

    XENEX LightStrike Blackout Curtains are recalled due to inadequate protection against UV and ozone exposure. Bystanders in rooms during device operation may experience temporary skin reddening, eye irritation, nausea, and headache.

    Product
    LightStrike Blackout Curtains, Part numbers; 610-00008, 610-00009, 610-00019, 610-00020, and 610-00024, used with the LightStrike Germ-Zapping Robots Models: PXUV4D, PXUV5D, LSMUV6-FT, or LSMUV6-SL, for whole room microbial reduction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1305-2024·2024-03-27

    Conductive Adhesive Gel Recalled Due to Thickness and Discoloration Issues

    Natus Neurology is recalling TENSIVE Conductive Adhesive Gel (Lot A0623009) after complaints of improper thickness, discoloration, and in one case, patient skin irritation following use.

    Product
    TENSIVE Conductive Adhesive Gel, REF 016-401600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1306-2024·2024-03-27

    Natus Sleep Supplies Recalled for Conductive Adhesive Gel Quality Defects

    Natus Neurology is recalling Sleep Supplies Start Kits due to defective conductive adhesive gel supplied by Parker Laboratories. The gel is too thick, discolored, and caused patient irritation in at least one case.

    Product
    natus neurology, Sleep Supplies Start Kit with Single Use Supplies for Embla EX Series Amplifiers, REF 024252
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24043·2023-12-07

    Wet & Forget Xtreme Reach Stain Remover with Hose End Nozzle Recalled

    Wet & Forget USA is recalling about 2.7 million bottles of "Xtreme Reach" Outdoor Mold & Mildew Stain Remover with hose end nozzles. The nozzle clip can dislodge, spraying cleaning solution on users and causing skin and eye irritation.

    Product
    Wet & Forget "Xtreme Reach" Outdoor Rapid Application Moss, Mold, Mildew & Algae Stain Remover with Hose End Nozzle
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23252·2023-08-03

    Maggie's Farm Aerosol Bed Bug & Flea Killer Cans Due to Rupture Hazard

    Maggie's Farm Ltd. is recalling about 14,500 units of its 14-ounce Bed Bug & Flea Killer aerosol cans because they can rupture and expel shrapnel, posing injury and laceration hazards. The firm has received four reports of ruptures but no injuries have been reported.

    Product
    Maggie's Farm 14 oz Bed Bug & Flea Killer
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0237-2023·2022-11-30

    Mighty Bliss Electric Heating Pad Recalled for Burn and Shock Risk

    Whele LLC is recalling the Mighty Bliss Electric Heating Pad due to burn and shock hazards. The company has received complaints of burns, electrical shocks, and skin irritation.

    Product
    Mighty Bliss Electric Heating Pad, Extra-Large (20 x 24 ) Blue Electric Heating Pad, MB-002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0238-2023·2022-11-30

    Mighty Bliss Electric Heating Pad recalled due to burn and shock hazard

    Whele LLC is recalling approximately 4,034 Mighty Bliss Electric Heating Pads due to burn and shock hazards. The firm received complaints of burns, mild electrical shocks, and skin irritation.

    Product
    Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Grey Electric Heating Pad, PE-MtyBls-HeatPad-12x24-Gry-V2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·23035·2022-11-03

    AirWick Fresh New Day Aerosol Air Fresheners Recalled for Rupture and Laceration Risk

    Reckitt is recalling about 67,000 AirWick Fresh New Day aerosol air fresheners in Fresh Linen and Fresh Waters scents due to a missing corrosion inhibitor in one batch that can cause cans to rupture or leak. No injuries have been reported.

    Product
    AirWick Fresh New Day® aerosol air fresheners - "Fresh Linen" and "Fresh Waters" scents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22190·2022-07-28

    Aesop Bathroom Deodorizer Drops and Oil Burner Blends Recalled

    Aesop USA is recalling Aesop Post-Poo Drops and four Aesop Oil Burner Blend products because their packaging does not meet child-resistant requirements and labels lack mandatory safety information, posing a poisoning risk.

    Product
    Aesop Post-Poo Drops and Aesop Oil Burner Blends
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0018-2022·2021-10-27

    Cleaning Solutions Foaming Hand Sanitizer Recalled for Skin Irritation Risk

    Sanitor Corporation is recalling Cleaning Solutions Foaming Hand Sanitizer (Benzalkonium chloride 0.1%) due to contamination from Current Good Manufacturing Practice (CGMP) deviations. Use may cause skin or soft tissue infection and irritation.

    Product
    Cleaning Solutions Foaming Hand Sanitizer, Active Ingredient Benzalkonium chloride 0.1%, New Wave Cleaning Solutions LLC, 7001 W Arby Ave Suite 100, Las Vegas, NV 89113, UPC#: 8 60001 93396 3
    Category
    Drug
    Distribution
    1 state
  • ModerateCPSC·21185·2021-08-18

    Primark Recalls 8-Pack Scent Stamper Pens for Elevated Benzyl Alcohol

    Primark is recalling about 9,500 8-pack Scent Stamper Pens due to elevated levels of benzyl alcohol in the purple pen, which poses a risk of skin irritation. No injuries have been reported.

    Product
    8-Pack Scent Stamper Pens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21768·2021-07-27

    Oculus Quest 2 Removable Foam Facial Interfaces Due to Skin Irritation Risk

    Facebook Technologies is recalling about 4 million removable foam facial interfaces for Oculus Quest 2 virtual reality headsets because the foam can cause facial skin irritation and reactions. Consumers should stop using affected interfaces and contact the manufacturer for a free silicone replacement.

    Product
    Removable Foam Facial Interfaces for Oculus Quest 2 Virtual Reality Headsets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21082·2021-02-17

    Primark Recalls Nose Piercings and Body Bars Due to Nickel Levels

    Primark is recalling 5-pack nose piercings and body bars because they contain high levels of nickel, posing a risk of skin irritation.

    Product
    5-Pack Nose Piercings and Body Bars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20160·2020-08-05

    WD-40 Recalls X-14 Mildew Stain Remover Due to Skin Irritation Risk

    WD-40 Company is recalling specific 16 and 32-ounce bottles of X-14 Mildew Stain Remover because pressure buildup may cause leaks and skin irritation.

    Product
    X-14® Mildew Stain Remover
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·20127·2020-05-27

    Primark Recalls Kitten Heel Court Shoes Due to Chromium Levels

    Primark is recalling Wide Fit Kitten Heel Court Pumps because the leather insoles contain elevated levels of Chromium VI, posing a risk of skin irritation.

    Product
    Wide Fit Kitten Heel Court Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide