The Recall Desk

Hazard

Sharp Edges recalls

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

What the numbers show

Total
132
Critical
1
Severe
6
Most recent
2026-06-09

Of the 132 sharp edges recalls we have scored against our rubric, 1 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 6 (5%) 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 sharp edges 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.

101–125 of 132

  • HighNHTSA·17V675000·2017-10-25

    Audi Recalls A4 and A5 Models for Loose Door Speaker Trim

    Volkswagen Group of America is recalling 2017-2018 Audi A4 and A5 vehicles because loose aluminum door trim can expose sharp edges, increasing the risk of injury to occupants.

    Product
    AUDI — AUDI A5, A4 ALLROAD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1814-2017·2017-04-19

    Aesculap Minop InVent 30 Trocar System Recalled for Sharp Edges

    Aesculap Implant Systems LLC is recalling the Minop InVent 30 Trocar System because sharp edges may abrade insulation during use.

    Product
    AESCULAP MINOP InVent 30 Trocar System, non-sterile Product Usage:The Minop InVent Trocar System intended use is for endoscopic procedures within the central nervous system, especially for the treatment of intra- and paraventricular pathological structures.
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·15007·2014-10-15

    Toys R Us Recalls Toy Toaster Sets Due to Choking Hazard

    Toys R Us is recalling Just Like Home toy toaster sets because the plastic toast can break into sharp pieces, posing a choking hazard.

    Product
    Just Like Home Toy Toaster Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0727-2014·2014-01-22

    Anspach Carbide Cutting Burrs Recalled Due to Fracture During Use

    The Anspach Effort, Inc. is recalling specific carbide cutting burrs because some fractured during use. The devices are intended for cutting and shaping bone.

    Product
    Anspach Carbide Cutting Burrs: 1.5MMx7.5MM Cylindrical Carbide Drum part # S-15DRMC-L, 1MM Carbide Fluted ball, Extended part # S-1B-C, 1MM Carbide Fluted ball part # S-SB-C, 2MM Carbide Fluted ball part # S-2SB-C, 3MM Carbide Fluted ball Extended part # S-3B-C, 3MM Carbide Flut
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0930-2013·2013-03-20

    Siemens ACUSON S2000 ABVS Scanner Recalled for Sharp Transducer Edges

    Siemens is recalling 214 ACUSON S2000 ABVS systems because the transducer pod may contain sharp edges that could cause injury.

    Product
    ACUSON S2000 Automated Breast Volume Scanner (ABVS); Model number 10042541 Distributed by Siemens Medical Solutions USA Inc. business Unit: Ultrasound. The S2000 Automated Breast Volume Scanner (ABVS) Ultrasound System for imaging of the breast allows volumetric acquisitio
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0908-2013·2013-03-13

    Medtronic DPL Single Stage Venous Cannula Recalled for Rough Metal Edges

    Medtronic is recalling DPL Single Stage Venous Cannulas used in cardiopulmonary bypass due to potential rough metal edges on the tip side ports.

    Product
    Medtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedures. Model numbers: 67312; 67314; CB67314; 67316; 67318; CB67318; 67320; 69312; 69314; 69316; 69318; 69320; 69322; 69324; 69328; 69331.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0892-2013·2013-03-13

    Ad-Tech Macro Micro Subdural Electrodes Recalled for Sharp Edges

    Ad-Tech Medical Instrument Corporation is recalling Macro Micro Subdural Electrodes because they may have sharp edges or fracture, posing a risk of injury to brain tissue.

    Product
    Ad-Tech Medical Instrument Corporation Macro Micro Subdural Electrode. For temporary (<30 days) use with recording, monitoring and stimulation equipment, for the recording, monitoring and stimulation of electrical signals on the surface level of the brain. The recording of elect
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0594-2013·2013-01-02

    Zimmer Spine Ardis Inserter Recalled for Potential Spacer Fragmentation

    Zimmer, Inc. is recalling the Spine Ardis Inserter because excessive force can break the PEEK spacer, causing sharp fragments that may damage adjacent structures.

    Product
    Zimmer Spine Ardis Inserter, Rx, non-sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2226-2012·2012-08-29

    Beckman Coulter DxH Slidemaker Stainer Floor Stand Recall for Sharp Edges

    Beckman Coulter is recalling 41 DxH Slidemaker Stainer Floor Stands because missing vinyl caps expose sharp edges on drawer slides, posing a physical injury risk to operators.

    Product
    UniCel DxH Slidemaker Stainer Stainer Floor Cabinet, PN A96152. The DxH Slidemaker Stainer is a fully automated slide preparation and staining device that aspirates a whole blood-sample, smears a blood film on a clean microscope slide, and delivers a variety of fixatives, stai
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2225-2012·2012-08-29

    Beckman Coulter DxH Slidemaker Stainer Floor Stand Recall for Sharp Edges

    Beckman Coulter is recalling 41 DxH Slidemaker Stainer Floor Stands because missing vinyl caps expose sharp edges on drawer slides, posing a physical injury risk to operators.

    Product
    UniCel DxH Slidemaker Stainer Instrument System, PN 775222. The DxH Slidemaker Stainer is a fully automated slide preparation and staining device that aspirates a whole blood-sample, smears a blood film on a clean microscope slide, and delivers a variety of fixatives, stains,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·12V247000·2012-05-30

    Keystone Vantage Recalled for Sharp Edges Near Holding Tank Valves

    Keystone is recalling 2012-2013 Vantage RVs because missing protective molding on sharp metal edges near holding tank valves can cause cuts to hands and arms.

    Product
    KEYSTONE — KEYSTONE VANTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·09742·2009-05-13

    Fushin USA Recalls Youth ATVs Due to Injury Risk

    Fushin USA is recalling about 650 youth ATVs because they lack front brakes and padding, posing an injury risk to young riders.

    Product
    Fushin ATVs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·08333·2008-07-17

    SunL Group Recalls SLA90 Youth ATVs Due to Safety Defects

    SunL Group Inc. is recalling approximately 144 SLA90 Youth ATVs because they lack front brakes, a manual fuel shut-off, and handlebar padding, posing a risk of serious injury.

    Product
    SLA90 Youth All-Terrain Vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·08519·2007-11-21

    Paricon Snow and Sand Castle Kits Recalled for Sharp Edges

    Paricon is recalling Snow and Sand Castle Kits sold at L.L. Bean because the largest block maker can crack, creating sharp edges that pose a laceration hazard to children.

    Product
    Snow and Sand Castle Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·08065·2007-11-06

    Swimways Recalls Skippy Pool Toys Due to Laceration Hazard

    Swimways Corp. is recalling Skippy Pool Toys because the elastic tongue can break and cut users' hands. Consumers should stop using the toys and contact the company for a replacement.

    Product
    Skippy Pool Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·04123·2004-04-20

    Kids II Recalls Vinyl Mirror Books Due to Laceration Hazard

    Kids II is recalling 225,000 vinyl children's books because the plastic mirrors can crack or break, posing a laceration hazard to young children.

    Product
    Vinyl Mirror Books
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·03043·2002-11-21

    Kolcraft Recalls Baby Walkers with Detachable Toy Attachments

    Kolcraft is recalling about 410,000 baby walkers because flower toys on the tray can detach, exposing sharp edges that pose a laceration hazard to young children.

    Product
    Toy Attachments on Baby Walkers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·00015·1999-11-10

    Perfecto Recalls SHOlights Aquarium Lights Due to Shock and Fire Risk

    Perfecto Manufacturing is recalling SHOlights aquarium lights because sharp edges may damage wiring, posing risks of electric shock, electrocution, or fire.

    Product
    SHOlights aquarium lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide