Hazard

Laceration recalls

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

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all laceration 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.

76–100 of 158

SevereFDA (Devices)·Z-0929-2024·2024-02-14
BrightView Gamma Camera Detector May Fall and Injure Patients
Philips BrightView gamma camera detectors may fall due to component failure, potentially causing patient injury including lacerations and fractures. The FDA is recalling all affected units.
Product
BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791 453560279811 453560279801; 4x4 digit format 2170-3000A 2170-3001A 2170-3002A 2170-3003A
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·24110·2024-02-08
Frigidaire Side-by-Side Refrigerators Recalled for Choking and Laceration Hazards
Electrolux Group is recalling about 383,240 Frigidaire side-by-side refrigerators with slim ice buckets because the ice bucket assembly can break and release plastic pieces that pose choking and laceration hazards.
Product
Frigidaire Branded Side by Side Refrigerators with Slim Ice Buckets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0953-2024·2024-02-07
MRI Scanner Quadrature Coil Seal Failure Poses Patient Contact Risk
Philips is recalling the Intera 1.5T Achieva Nova-Dual MRI scanner due to potential failure of the Quadrature Body Coil seal adhesive. If the seal fails, sharp edges may contact patients, risking skin injuries.
Product
Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0952-2024·2024-02-07
Philips MRI Scanner Quadrature Coil Seal Adhesive May Fail and Create Sharp Edges
Philips Intera 1.5T Achieva Nova MRI machines (Model 781172) may develop seal adhesive failure in the Quadrature Body Coil, creating sharp edges that could injure patients during scanning.
Product
Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0946-2024·2024-02-07
Achieva 1.5T MRI Coil Seal Adhesive May Fail Creating Sharp Edges
Philips Achieva 1.5T MRI scanner components may experience coil seal adhesive failure, creating sharp edges that could injure patients. Affected devices have been distributed worldwide.
Product
Achieva 1.5T Conversion. Model (REF) Numbers 781346, 781283.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0945-2024·2024-02-07
Philips Achieva MRI Scanner Recall: Loose Coil Seals May Cause Skin Injury
Philips is recalling Achieva 1.5T MRI scanners due to a seal adhesive defect on the body coil that may fail during scanning, creating sharp edges that risk skin injury including abrasions and lacerations.
Product
Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0951-2024·2024-02-07
Philips Ingenia 3.0T CX MRI: Loose Coil Seal May Cause Sharp Edges
Philips is recalling Ingenia 3.0T CX MRI machines due to potential failure of the Quadrature Body Coil seal adhesive. Loose seals may create sharp edges that risk skin injury or hair entanglement during scanning.
Product
Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0947-2024·2024-02-07
Philips Achieva 1.5T MRI system recalled for defective coil seal
Philips is recalling the Achieva 1.5T Initial MRI system due to a defective Quadrature Body Coil seal. The adhesive may fail and create sharp edges that could cut or abrade patients during scanning.
Product
Achieva 1.5T Initial system. Model (REF) Numbers 781178.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0948-2024·2024-02-07
Philips Achieva 3.0T MRI Coil Seal Adhesive May Fail, Risking Patient Injury
The Quadrature Body Coil seal adhesive in Philips Achieva 3.0T MRI scanners may fail, creating sharp edges that can injure patients. All units with model numbers 781277, 781177, 781278, 781344, and 781345 are affected.
Product
Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0954-2024·2024-02-07
MRI Machine Coil Seal Adhesive May Create Sharp Edges
The Intera Achieva 1.5T Pulsar MRI machine's Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients. All units of this model are affected.
Product
Intera Achieva 1.5T Pulsar. Model (REF) Number 781171.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0950-2024·2024-02-07
Philips Ingenia MRI Scanner Body Coil Seal Adhesive May Fail
Philips is recalling Ingenia 1.5T CX MRI scanners because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients. Model numbers 781262 and 781261 are affected.
Product
Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0955-2024·2024-02-07
Philips MRI Coil Seal Adhesive May Fail and Create Sharp Patient Contact Surfaces
Philips has recalled certain SmartPath to dStream MRI coil components because the seal adhesive may fail, creating sharp edges that could contact patients during scanning and cause skin and tissue injuries.
Product
SmartPath to dStream for 1.5T. Model (REF) Numbers 781260, 782112.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0949-2024·2024-02-07
Philips Achieva XR MRI Coil Seal Adhesive Failure Risk
Philips Achieva XR MRI body coil seal adhesive may fail and create sharp edges that could injure patients. Affected units are being recalled.
Product
Achieva XR. Model (REF) Numbers 781153, 781253.
Category
Medical Device
Distribution
Distributed nationwide
ModerateCPSC·24106·2024-02-01
Glass Little Wanderer Snow Globes Recalled for Laceration Hazard
The Museum of Modern Art is recalling about 1,915 glass Little Wanderer snow globes sold at MoMA Design Stores because they can crack or fracture, posing a laceration hazard. No injuries have been reported.
Product
Snow globes (Little Wanderer)
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·24099·2024-02-01
Meijer December Home Light Bulbs Recalled for Burst Hazard
Meijer is recalling December Home branded candelabra-style light bulbs because some packages contain 3V bulbs instead of the labeled 120V versions. When a 3V bulb is used in a 120V fixture, it can burst, creating a laceration hazard.
Product
DECEMBER HOME® Replacement Light Bulbs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0679-2024·2024-01-17
Gamma Camera Recalls Due to Potential Patient Extremity Entrapment Hazard
Philips BrightView XCT gamma cameras may pose an extremity entrapment hazard during certain scanning operations. A gap can form between the patient support and detector, risking fractures, lacerations, and crush injuries.
Product
BrightView XCT, Gamma Camera, Product Code 882482
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0677-2024·2024-01-17
Philips BrightView Gamma Camera System Recalled for Extremity Entrapment Hazard
Philips is recalling BrightView Gamma Camera Systems because a gap can form between patient support and detector during quality assurance scans, creating an extremity entrapment hazard that may cause fractures or crush injuries.
Product
BrightView, Gamma Camera System, Product Code 882480.
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·24069·2023-12-28
BlendJet Recalls 4.8 Million BlendJet 2 Portable Blenders for Fire and Laceration Risk
BlendJet Inc. is recalling approximately 4.8 million BlendJet 2 Portable Blenders because they can overheat, catch fire, or have blades that break off during use, creating fire and laceration hazards.
Product
BlendJet 2 Portable Blenders
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24725·2023-11-30
Klickpick Home Children's Cup Sets Recalled for Lead and Choking Hazards
Klickpick Home is recalling about 3,600 stainless steel children's cup sets sold on Amazon from March through September 2023. The cups contain lead-bearing solder that exceeds federal limits, and the lids can crack and produce sharp edges and small parts.
Product
Klickpick Home Children's Cup Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24724·2023-11-30
Tiblue Children's Cups Recalled for Lead Content and Lid Hazards
Tiblue 8 oz and 12 oz stainless steel children's cups are being recalled because they contain lead in solder on the bottom exterior that exceeds federal limits, and the lids can crack and break during use, creating sharp edges and choking hazards.
Product
Tiblue 8 oz and 12 oz children's cups
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24710·2023-11-09
Magnolia Market Recalls 3-Wick Glass Candles Due to Fire and Laceration Hazards
Magnolia Market recalled 3-Wick Glass Candles (batch 120122) due to incorrect wax causing excessive flames and glass breakage. 13 incidents reported with minor property damage in 4 cases; no injuries.
Product
Magnolia 26 oz. 3-Wick Glass Candles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24024·2023-11-09
IKEA LETTAN Mirrors Expanded Recall Due to Laceration Hazard
IKEA is expanding a recall of LETTAN flat mirrors because plastic wall fittings can break and cause the mirror to fall, creating a laceration hazard. No injuries have been reported.
Product
IKEA LETTAN Mirrors
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24016·2023-11-02
Grizzly Industrial Wood Lathes Recalled for Projectile and Laceration Hazards
Grizzly Industrial and Shop Fox wood lathes are being recalled because the cutting tool can break, creating a risk of projectiles striking users or bystanders, and lacerations to users. About 21,300 units are affected.
Product
Grizzly Industrial and Shop Fox Wood Lathes
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24706·2023-10-26
Bobcat and Kubota Stand-On Zero-Turn Lawnmowers Recalled for Crash and Laceration Hazard
Doosan Bobcat North America is recalling about 830 Bobcat- and Kubota-branded stand-on zero-turn lawnmowers due to a steering system defect that can prevent the control levers from returning to neutral, disabling the operator presence switch and stopping mechanism. This poses crash and laceration hazards.
Product
Bobcat-branded and Kubota-branded stand-on zero-turn lawnmowers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24008·2023-10-12
Gevi Countertop Nugget Ice Makers Recalled Due to Laceration Hazard
Gevi countertop nugget ice makers with model number GIMN-1102 and a date code before June 1, 2022, are being recalled because metal auger blades can break and create sharp metal pieces in the ice basket, posing a laceration risk. No injuries have been reported.
Product
Gevi Household Countertop Nugget Ice Makers
Category
Consumer Product
Distribution
Distributed nationwide