Recalls in December 2025 (page 4)
421 recalls.
- MAXXUS recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 21, 2026 · GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and ... - SMV BodyTrack recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 21, 2026 · GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and ... - SMV DSI recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 21, 2026 · GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and ... - SMV DSX New Line recall (GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING)
Medical deviceClass IIReported January 21, 2026 · GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and ... - A71200 Vanta" Clinician Programmer Application recall (Medtronic Neuromodulation)
Medical deviceClass IIReported January 21, 2026 · Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure. - Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter recall (Boston Scientific Corporation)
Medical deviceClass IIReported January 21, 2026 · Boston Scientific is initiating the removal of certain batches of Coyote" Over-the-Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation... - Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography recall (Mobius Imaging, LLC)
Medical deviceClass IIReported January 21, 2026 · AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label. - Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography recall (Mobius Imaging, LLC)
Medical deviceClass IIReported January 21, 2026 · AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label. - MAVERICK¿ Measurement Module Spectrometer PN 820-01367 recall (REPLIGEN CORPORATION)
Medical deviceClass IIReported January 21, 2026 · Potential Elevated Laser Output A disconnected cable or a poorly crimped cable under mechanical bending stress can cause loss of electrical contact. At one... - VANTAGE TITAN 3T Model MRT-3010/MEXL-3010 recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported January 21, 2026 · There is a potential for formation of ice occurring in the venting system of the superconducting magnet of the MRI systems. if a quench occurs in this... - VANTAGE GALAN 3T Model MRT-3020/MEXL-3020 recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported January 21, 2026 · There is a potential for formation of ice occurring in the venting system of the superconducting magnet of the MRI systems. if a quench occurs in this... - Bengal King Jhal Chanachur food treats 12.34oz recall (South Asian Food Inc.)
FoodClass IReported January 14, 2026 · Contains undeclared peanuts - MARKET 32 by Price Chopper brand recall (DIRECT SOURCE SEAFOOD LLC)
FoodClass IIReported January 14, 2026 · Shrimp may be contaminated with Cesium-137 (Cs-137). - waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal 8-12 Count... recall (DIRECT SOURCE SEAFOOD LLC)
FoodClass IIReported January 14, 2026 · Shrimp may be contaminated with Cesium-137 (Cs-137). - Baraka Gourmet Pastry Kunafe 6.7oz. recall (ZIYAD BROTHERS IMPORTING)
FoodClass IIReported January 14, 2026 · May contain partially hydrogenated oils - Baraka French Style Puff Pastry 1lb and 1.5lbs sizes recall (ZIYAD BROTHERS IMPORTING)
FoodClass IIReported January 14, 2026 · May contain partially hydrogenated oils - Sysco Imperial Potato Tater Barrel recall (McCain Foods USA Inc)
FoodClass IIReported January 14, 2026 · Clear hard plastic fragments. - Ore-Ida Tater Tots shaped potatoes recall (McCain Foods USA Inc)
FoodClass IIReported January 14, 2026 · Clear hard plastic fragments. - Sapori Amaretti Almonds 175 g Cookies recall (D. Coluccio & Sons Inc.)
FoodClass IIReported January 14, 2026 · Contains elevated levels of hydrocyanic acid - Tita Crackers Rovira recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Vainilla Crackers recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Vanilla Treats Crackers recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Vanilla Econo recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Tempting Crackers Tray recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Snack Crackers 100to en boca recall (Rovira Biscuit Corporation)
FoodClass IIReported January 14, 2026 · Undeclared colors FD&C Yellow #6, and FD&C Red 40 - Sam Dry Fruits & Nuts PISTACHIO Meats Whole LOT #: PK00459 recall (Sam Dry Fruits and Nuts Enterprises, Inc)
FoodClass IReported January 14, 2026 · Potential contamination with Salmonella. - Eggs Potatoes Cheese Tacos recall (Fresh & Ready Foods LLC)
FoodClass IIReported January 14, 2026 · Foreign material. - Spicy Egg Potatoes Cheese Tacos recall (Fresh & Ready Foods LLC)
FoodClass IIReported January 14, 2026 · Foreign material. - Spicy Breakfast Burrito recall (Fresh & Ready Foods LLC)
FoodClass IIReported January 14, 2026 · Foreign material. - Spicy Veggie Breakfast Burrito recall (Fresh & Ready Foods LLC)
FoodClass IIReported January 14, 2026 · Foreign material. - Lunds & Byerlys Monster Cookies recall (Lund Food Holdings Inc)
FoodClass IReported January 14, 2026 · Undeclared allergens (Peanut, Egg, Soy) - Rosuvastatin Tablets recall (AvKARE)
DrugClass IIReported January 14, 2026 · Out of specification for dissolution. - ClearLife Allergy Nasal Spray recall (Medinatura New Mexico, inc.)
DrugClass IReported January 14, 2026 · Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. - ReBoost Nasal Spray recall (Medinatura New Mexico, inc.)
DrugClass IReported January 14, 2026 · Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. - Oxycodone and Acetaminophen CII Tablets USP recall (SpecGx, LLC)
DrugClass IIReported January 14, 2026 · Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets. - Oxycodone and Acetaminophen CII Tablets USP recall (SpecGx, LLC)
DrugClass IIReported January 14, 2026 · Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets. - ORL Kids Natural Toothpaste recall (Signature Formulations, LLC)
DrugClass IIReported January 14, 2026 · cGMP Deviations - ORL Kids Mouthwash recall (Signature Formulations, LLC)
DrugClass IIReported January 14, 2026 · cGMP Deviations - Tri-Moxi+¿ recall (Imprimis NJOF, LLC)
DrugClass IIReported January 14, 2026 · Presence of particulate matter - Glass like particles. - Dexamethasone Moxifloxacin Ketorolac recall (Imprimis NJOF, LLC)
DrugClass IIReported January 14, 2026 · Presence of particulate matter - Glass like particles. - Dexamethasone Moxifloxacin recall (Imprimis NJOF, LLC)
DrugClass IIReported January 14, 2026 · Presence of particulate matter - Glass like particles. - Fesoterodine Fumarate recall (Alembic Pharmaceuticals Limited)
DrugClass IIIReported January 14, 2026 · Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit. - Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Codman CereLink... recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported January 14, 2026 · Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits. - Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN... recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported January 14, 2026 · Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits. - Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number:... recall (IMRIS Imaging Inc)
Medical deviceClass IIReported January 14, 2026 · Torque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision, procedural delays... - Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor. recall (Philips North America Llc)
Medical deviceClass IIReported January 14, 2026 · It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength... - Arial 900 MHz Call Station recall (Securitas Healthcare LLC)
Medical deviceClass IIReported January 14, 2026 · Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1)... - Arial 900 MHz Call Station recall (Securitas Healthcare LLC)
Medical deviceClass IIReported January 14, 2026 · Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1)... - Impella 5.5 with SmartAssist¿ S2 recall (Abiomed, Inc.)
Medical deviceClass IIReported January 14, 2026 · Device packaged in incorrect outer box carton. - BD Pyxis ES Enterprise Server Catalog Numbers 1115-00 recall (CareFusion 303, Inc.)
Medical deviceClass IIReported January 14, 2026 · Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems. - Revogene C. difficile recall (Meridian Bioscience Inc)
Medical deviceClass IIReported January 14, 2026 · The affected lots show a decline in performance over time, which may lead to false-negative results. - Kii Low Profile recall (Applied Medical Resources Corp)
Medical deviceClass IIReported January 14, 2026 · There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing. - Philips Incisive CT recall (Philips Healthcare (Suzhou) Co., Ltd.)
Medical deviceClass IIReported January 14, 2026 · Potential for incomplete scan due to unstable connection inside of floating sensor. - LUMINOS Lotus Max recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported January 14, 2026 · A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and... - Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Chocolate GF V. Product is... recall (Tom Bumble LLC)
FoodClass IIReported January 7, 2026 · Foreign material. - 1) Paw Patrol Heart-Shaped Gummy Candies recall (Bendon Publishing)
FoodClass IIIReported January 7, 2026 · Unapproved color additive - chlorophyllin copper complex - traZODONE Hydrochloride Tablets recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIIReported January 7, 2026 · Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface. - Ondansetron Orally Disintegrating Tablets recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIReported January 7, 2026 · Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets... - Wegovy recall (Novo Nordisk Inc.)
DrugClass IIReported January 7, 2026 · Presence of Particulate Matter: Hair was found in a prefilled syringe - Wegovy recall (Novo Nordisk Inc.)
DrugClass IIReported January 7, 2026 · Presence of Particulate Matter: Hair was found in a prefilled syringe - BD ChloraPrep" Triple Swabsticks recall (CareFusion 213, LLC)
DrugClass IIReported January 7, 2026 · Lack of Assurance of Sterlity - BVI Leos Laser and Endoscopy System. Model Number: OME6000U. recall (Beaver-Visitec International, Inc.)
Medical deviceClass IIReported January 7, 2026 · Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not... - 1) Wegmans Deluxe Mixed Nuts recall (Mellace Family Brands California Inc)
FoodClass IReported December 31, 2025 · Potential contamination with Salmonella - Publix Raspberry Coffee Cake recall (The James Skinner LLC)
FoodClass IIReported December 31, 2025 · Undeclared allergen - walnuts. Maple Walnut Coffee Cake was incorrectly labeled as Raspberry Coffee Cake and walnuts were not declared on the label. - Grandma Belle's Tomato Basil Soup recall (Lil Turtles LLC)
FoodClass IIReported December 31, 2025 · Undeclared allergen - milk - Noxafil Powdermix recall (Merck Sharp & Dohme LLC)
DrugClass IIReported December 31, 2025 · Presence of particulate matter: potential presence of metal particulates in the product. - Merck Emend recall (Merck Sharp & Dohme LLC)
DrugClass IIReported December 31, 2025 · Presence of particulate matter: potential presence of metal particulates in the product. - LYFO DISK recall (Microbiologics Inc)
Medical deviceClass IIReported December 31, 2025 · Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428. - KWIK-STIK 6-Pack recall (Microbiologics Inc)
Medical deviceClass IIReported December 31, 2025 · Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428. - KWIK-STIK 2-Pack recall (Microbiologics Inc)
Medical deviceClass IIReported December 31, 2025 · Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428. - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade... recall (Zimmer, Inc.)
Medical deviceClass IIReported December 31, 2025 · Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant... - Ciclopirox Shampoo recall (SUN PHARMA /TARO)
DrugClass IIReported December 24, 2025 · Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint - Meaicezli Play Purse Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Angeer-US
Consumer productReported December 24, 2025 · The children's toy violates the mandatory standard for toys because the toy cell phone contains button cell batteries and the toy tablet contains a lithium... - Blue Wave Recalls Above-Ground Pools 48 Inches and Taller Due to Drowning Hazard
Consumer productReported December 18, 2025 · The compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk. - SereneLife Home Recalls Above-Ground Pools 48 Inches and Taller Due to Drowning Hazard
Consumer productReported December 18, 2025 · This recall involves all SereneLife brand above-ground pools 48 inches and taller. Models SLPORND15 and SLPORND18 are included in this recall. Model... - ANNQUAN Brand Power Strips Recalled Due to Risk of Serious Injury or Death from Fire; Sold on Amazon by Hefei Juyuan Sporting Development
Consumer productReported December 18, 2025 · The power strips do not contain supplementary overcurrent protection, which creates a risk of fire if the power strips are overloaded. The resulting fire can... - JOKOSIS Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by JOKOSIS
Consumer productReported December 18, 2025 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped... - KKL Fabric 9-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by HK Brilliant
Consumer productReported December 18, 2025 · The recalled dressers are unstable if they are not anchored to the wall, posing a serious tip-over and entrapment hazards that can result in injuries or death... - Feel The Beard Recalls Minoxidil Beard Growth Serum Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported December 18, 2025 · The beard serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's packaging... - Plantimex Recalls Mamisan Lidocaine Ointment Containers Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported December 18, 2025 · The ointment contains lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The ointment's packaging is... - 17 Stories Furniture 18-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Imported by Shenzhen Jinhongzhen Technology Co
Consumer productReported December 18, 2025 · The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazard that can result in injuries or death to... - Currey & Company Recalls Electra Chandeliers Due to Impact Injury Hazard
Consumer productReported December 18, 2025 · The component that connects the recalled chandelier light fixture to the ceiling mount is not threaded properly and the fixture can fall unexpectedly, posing a... - TopHomer Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violation of the Virginia Graeme Baker Pool and Spa Safety Act; Sold on Amazon by TopHomerUS
Consumer productReported December 18, 2025 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and... - Furnulem 8-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Furnulem
Consumer productReported December 18, 2025 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in serious injuries or death to...