The Recall Desk

Hazard

Eye Injury recalls

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

What the numbers show

Total
71
Critical
0
Severe
27
Most recent
2026-07-30

Of the 71 eye injury recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 27 (38%) 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 eye injury 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.

26–50 of 71

  • SevereFDA (Devices)·Z-0502-2019·2018-12-05

    NxStage PureFlow B Solution Recalled for Potential Bag Bursting and Injury

    NxStage Medical is recalling specific lots of PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-402, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0503-2019·2018-12-05

    NxStage PureFlow B Solution Recalled Due to Bag Burst Risk

    NxStage Medical is recalling 2,189 units of PureFlow B Solution because the bag's smaller chamber can burst, releasing electrolyte fluid that may injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-403, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0504-2019·2018-12-05

    NxStage PureFlow B Solution Recalled for Potential Bag Burst Injury Risk

    NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-404, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0501-2019·2018-12-05

    NxStage PureFlow B Solution Recalled Due to Bag Burst Risk

    NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-401, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2916-2018·2018-08-29

    Johnson & Johnson Recalls 1-Day ACUVUE MOIST Contact Lenses

    Johnson & Johnson Vision Care is recalling specific lots of 1-Day ACUVUE MOIST contact lenses due to reports of partially formed lenses that appear smaller and stiffer.

    Product
    Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12 split lots, repackaged in 30 and 90-packs . Intended for daily disposable wear for the optical correction of refractive ametropia (myopia and hyperopia) in p
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13277·2013-09-06

    Crosman Recalls Air Pistols Due to Explosion Hazard

    Crosman is recalling specific air pistol models because they can explode at high temperatures, posing a risk of serious injury to users.

    Product
    Air pistols
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·11320·2011-09-08

    Target Recalls Embark Resistance Cords Due to Eye Injury Hazard

    Target is recalling approximately 447,000 Embark resistance cords because the door anchor ball can release and strike users, causing eye injuries.

    Product
    Embark Resistance Cords and Cord Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·10163·2010-03-11

    Hitachi Koki Recalls Coil Nailers Due to Sideways Ejection Hazard

    Hitachi Koki is recalling about 65,000 coil nailers because a faulty feeder may eject nails sideways, posing a serious injury risk to users and bystanders.

    Product
    Coil Nailers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·09043·2008-11-13

    Modell's Recalls CORAL Swim 'N Score Pool Stix Due to Impalement Risk

    Modell's Sporting Goods is recalling CORAL Swim 'N Score Pool Stix because children can suffer impalement injuries if they fall on the weighted plastic tubes in shallow water.

    Product
    CORAL Swim 'N Score Pool Stix
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·07250·2007-07-24

    Estes-Cox Recalls Sky Rangers Park Flyer Radio Control Airplanes

    Estes-Cox is recalling about 21,000 Sky Rangers Park Flyer radio control airplanes due to a risk of explosion near the user's head, which can cause hearing damage and injuries.

    Product
    Sky Rangers Park Flyer Radio Control Airplanes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·06090·2006-02-15

    Brass Eagle Paintball Markers Recalled for Ejecting CO2 Cartridges

    Brass Eagle is recalling Blade Turbo paintball markers because CO2 cartridges can eject and hit users. Seven injuries have been reported.

    Product
    Brass Eagle Blade Turbo Markers and Paintball Breakout Players Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·04065·2004-01-20

    K'NEX Recalls Mud Boggers and Street Shredders Pump Up Racers

    K'NEX is recalling about 14,000 Mud Boggers and Street Shredders Pump Up Racers because the air motor can burst, posing a risk of eye or laceration injuries.

    Product
    Mud Boggers and "Street Shredders" Pump Up Racers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·02237·2002-08-28

    Todson Recalls Topeak Joe Blow Comp Bicycle Floor Pumps

    Todson Inc. is recalling about 10,000 Topeak Joe Blow Comp bicycle floor pumps because the pressure gauge lens can detach and strike users.

    Product
    Bicycle Tire Floor Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·02142·2002-04-18

    Estes Air Powered Rocket Systems Recalled Due to Injury Risk

    Estes Industries is recalling GL-X200 Air Powered Rocket Systems because foam tips and pump handles can break, causing injuries.

    Product
    GL-X200™ Estes Air™ Powered Rocket Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·01197·2001-07-13

    JT USA Recalls Proteus Paintball Masks Due to Eye Injury Risk

    JT USA is recalling Proteus paintball masks because the plastic facemask could crack around the ear cover, potentially exposing consumers to eye injuries.

    Product
    Proteus paintball mask
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·00169b·2000-08-24

    Colorbök Gel Pens Recalled Due to Risk of Eye and Facial Injuries

    Colorbök is recalling gel pens included with Icee Black notebooks and notepads because the end caps can shoot off, posing a risk of eye and facial injuries.

    Product
    Gel pens included with Icee Black notebooks and Icee Black notepads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·00134·2000-06-27

    Galoob Recalls Sky Dancers Flying Dolls Due to Injury Risk

    Galoob Toys is recalling Sky Dancers flying dolls because they can fly unpredictably and strike people, causing injuries.

    Product
    Sky Dancer® flying dolls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·98150·1998-08-18

    Brass Eagle Recalls Xtreme Vision 280 Paintball Masks Due to Lens Cracking

    Brass Eagle is recalling about 42,300 paintball masks because the lenses can crack when struck by a paintball, posing a potential eye injury hazard.

    Product
    Brass Eagle's Z Leader Xtreme Vision 280 paintball masks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·98100·1998-04-27

    Schutt Recalls Baseball and Softball Training Aids Due to Injury Risk

    Schutt Manufacturing is recalling about 12,000 Baseball and Softball Striker training aids because the ball can detach from the cable during use, posing a risk of serious injury to users and bystanders.

    Product
    Baseball and Softball Training Aids Recalled by Schutt Manufacturing
    Category
    Consumer Product
    Distribution
    Distributed nationwide