Recalls in June 2026 (page 4)
405 recalls.
- BD ChloraPrep CLear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep CLear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Scrub Teal recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Scrub Teal recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - ChloraPrep FREPP recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD PurPrep recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - BD ChloraPrep Hi-Lite Orange recall (CareFusion 213, LLC)
DrugClass IIReported July 8, 2026 · Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to... - Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems... recall (Zimmer Surgical Inc)
Medical deviceClass IIReported July 8, 2026 · Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result... - Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems... recall (Zimmer Surgical Inc)
Medical deviceClass IIReported July 8, 2026 · Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result... - MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number:... recall (BD SWITZERLAND SARL)
Medical deviceClass IIReported July 8, 2026 · Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market. - Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557 recall (Carl Zeiss Meditec AG)
Medical deviceClass IIReported July 8, 2026 · Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications. - ARTIS icono ceiling. Model Number: 11328100. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Over time some screws that keep the monitor attached to the... - Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog... recall (Medela Inc)
Medical deviceClass IIReported July 8, 2026 · May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery... - Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer recall (Accuray Incorporated)
Medical deviceClass IIReported July 8, 2026 · In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the... - Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer recall (Accuray Incorporated)
Medical deviceClass IIReported July 8, 2026 · In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the... - GC Agar Base recall (Remel, Inc)
Medical deviceClass IIReported July 8, 2026 · Reduced or no recovery of some strains of Neisseria gonorrhoeae. - Dried Herring Fish 7 oz. recall (Prime Food Processing LLC.)
FoodClass IReported July 1, 2026 · Improperly eviscerated which may result in Clostridium botulinum contamination - Perampanel CIII Tablets recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported July 1, 2026 · Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets. - Povi-One recall (Elevate Oral Care)
DrugClass IIReported July 1, 2026 · sub potency - Lacosamide Tablets recall (Annora Pharma Private Limited)
DrugClass IIReported July 1, 2026 · Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg. - hydrOXYzine Hydrochloride Oral Solution recall (ANI Pharmaceuticals, Inc.)
DrugClass IIIReported July 1, 2026 · Presence of foreign substance - Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag recall (Central Admixture Pharmacy Services, Inc.)
DrugClass IIReported July 1, 2026 · Incorrect product formulation: bag did not contain copper and famotidine per label. - DULOXETINE D/R recall (Direct Rx)
DrugClass IIReported July 1, 2026 · CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Corlanor recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · Presence of Foreign Substance. - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Corlanor recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · Presence of Foreign Substance. - Carton Label: MAJOR recall (The Harvard Drug Group LLC)
DrugClass IIReported July 1, 2026 · Subpotent Drug - Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following... recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure... - Combination Smoke and Carbon Monoxide (CO) Detectors Recalled Due to Risk of Serious Injury or Death from Failure to Alert Consumers to Fire; Sold Exclusively on Amazon.com by Treatlife Technology
Consumer productReported June 30, 2026 · The recalled detectors can fail to alert consumers of a fire, posing a risk of serious injury or death from smoke inhalation or burns. - Daikin Comfort Technologies Manufacturing Recalls Amana Air Conditioners and Heat Pumps Due to Risk of Serious Injury from Fire and Burns
Consumer productReported June 30, 2026 · The heating element can remain energized during a ground fault, despite being turned off, posing a risk of fire or burn injury to consumers. - Honlyne LED Party Favors Recalled Due to Risk of Serious Injury Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries; Sold by Huizhou Rongheng Network Technology
Consumer productReported June 30, 2026 · The LED party favors violate the mandatory safety standard for consumer products because the battery compartment within the light-up products contains button... - Montessori Busy Board Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Small Fish
Consumer productReported June 30, 2026 · The busy boards violate the mandatory safety standard for toys because magnets can detach, posing a deadly ingestion hazard. When high-powered magnets are... - Raychy Children's Light Sneakers Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries; Imported by Carina and Rambo
Consumer productReported June 30, 2026 · The recalled sneakers violate the mandatory standard for consumer products with button cell and coin batteries because the lithium coin batteries can be... - Shield Line Recalls MedPride Baby Oil Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Consumer productReported June 30, 2026 · The baby oil contains low-viscosity hydrocarbons, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The baby... - Southern Telecom Expands Recall of Lomi Waxing Kits Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Additional Model and Reported Incidents
Consumer productReported June 30, 2026 · The roll-on warmers' power cord can overheat and short circuit, posing a risk of serious injury or death from fire, burn and electrical shock hazards. - Super Off-Road Solar Power Banks Recalled Due to Overheating; Imported by Spector & Co.
Consumer productReported June 30, 2026 · The solar power bank's lithium-ion battery can swell and overheat, posing a burn hazard to consumers. - Yamazuki Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash; Violate Mandatory Standard for ATVs
Consumer productReported June 30, 2026 · The recalled youth ATVs violate the mandatory safety standard for ATVs because they are missing brake lights, reducing visibility of the youth ATV to other... - Kith Retail Recalls Children's Loungewear Sets Due to Risk of Serious Injury from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear
Consumer productReported June 30, 2026 · The recalled children's loungewear sets violate the mandatory flammability standards for children's sleepwear, posing a risk of serious burn injuries. - Al Yaman Halawa Extra Pistachio 907g recall (GREENWORLD FOOD EXPRESS (USA) LLC)
FoodClass IReported June 24, 2026 · Product may be contaminated with Salmonella - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Cura Hongos recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Rapidol recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Lil Drug Store recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Circle K recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Lucky Super Soft recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Lucky Super Soft recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Chlorthalidone Tablets recall (Inventia Healthcare Limited)
DrugClass IIReported June 24, 2026 · Failed Dissolution Specifications - Focalin XR recall (Sandoz Inc)
DrugClass IIIReported June 24, 2026 · Labeling: Incorrect or Missing Lot and/or Exp Date - Buprenorphine HCl recall (Par Health USA, LLC)
DrugClass IIReported June 24, 2026 · Crystallization; identified as Buprenorphine free base - Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products
Consumer productReported June 18, 2026 · The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the... - Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury from Fall Hazard
Consumer productReported June 18, 2026 · The recalled car seat adapters can fail to properly attach to the stroller, which may allow the car seat to fall, posing a risk of serious injury from a fall... - SHEIN Distribution Corporation Recalls Michley Children's Pajamas Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Children's Sleepwear
Consumer productReported June 18, 2026 · The recalled children’s pajamas violate the mandatory flammability standard for children’s sleepwear, posing a risk of serious burn injuries or death. - Bada Boom Fireworks Recalls Pyro Diablo "Diablo Rising" Fireworks Due to Risk of Serious Injury or Death from Explosion and Burn Hazards; Violate Fireworks Ban
Consumer productReported June 18, 2026 · The recalled fireworks violate the ban for aerial fireworks devices intended to produce audible effects because they have a pyrotechnic composition that... - Arizer Solo III Portable Vaporizers Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by 7111495 Canada
Consumer productReported June 18, 2026 · The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns. - Veseacky Pajama Sets Recalled Due to Risk of Serious Injury Death from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear
Consumer productReported June 18, 2026 · The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns. - Spa Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Arrogantf
Consumer productReported June 18, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and... - GOPO Toys Recalls Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys
Consumer productReported June 18, 2026 · The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach... - BABESIDE Doll and Stroller Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban; Sold on Amazon by HYBDOLLS
Consumer productReported June 18, 2026 · The recalled toys violate the small parts ban because they are intended for children under three and the small pacifier poses a deadly choking hazard to young... - The Lover Loose-Leaf Tea - Tart Chocolaty Tisane recall (Wild Coast Brew LLC)
FoodClass IIIReported June 17, 2026 · Dry tea blends product containing Ashwagandha root which is an unsafe food additive. - The Creator Loose-Leaf Tea - Ginger Lemongrass Tisane recall (Wild Coast Brew LLC)
FoodClass IIIReported June 17, 2026 · Dry tea blends product containing Ashwagandha root which is an unsafe food additive. - The Shadow Loose-Leaf Tea - Winter Spice Black Tea recall (Wild Coast Brew LLC)
FoodClass IIIReported June 17, 2026 · Dry tea blends product containing Ashwagandha root which is an unsafe food additive. - MMB of Louisiana Pasteurized Donor Human Milk recall (Mothers' Milk Bank of Louisiana at Ochsner Baptist)
FoodClass IIIReported June 17, 2026 · Potential physical contamination: dark spot was noticed on the bottom of container. - BEEKEEPER'S NATURALS Saline Nasal Spray recall (BEEKEEPER'S NATURALS USA INC.)
DrugClass IReported June 17, 2026 · Microbial Contamination of Non-Sterile Products - Minocycline Hydrochloride Extended-Release Tablets recall (Ascend Laboratories, LLC)
DrugClass IIReported June 17, 2026 · Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis - Gas-X Extra Strength recall (Haleon US Holdings LLC)
DrugClass IReported June 17, 2026 · Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process. - Primidone Tablets recall (Amneal Pharmaceuticals, LLC)
DrugClass IIIReported June 17, 2026 · Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer. - Duloxetine Delayed-Release Capsules recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported June 17, 2026 · CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit - Duloxetine Delayed-Release Capsules recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported June 17, 2026 · CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit - Coffeemakers Recalled Due to Risk of Serious Injury from Burn Hazard; Imported by Kidisle
Consumer productReported June 12, 2026 · The recalled coffeemakers can become clogged, causing hot liquid or steam to build up and be released unexpectedly during use, posing a risk of serious injury... - Yamaha Recalls UMAX Bistro and Bistro Deluxe Vehicles Due to Injury Hazard
Consumer productReported June 12, 2026 · The recalled Bistro and Bistro Deluxe vehicles have an inaccurate weight capacity certification label. This could result in the vehicle being overloaded, which... - Houoto 642-2150V Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Prosperity goes straight up
Consumer productReported June 12, 2026 · The drain covers do not bear the required product markings, in violation of the mandatory safety standard under the Virginia Graeme Baker Pool and Spa Safety... - Arctic Zone Titan Pro Coolers Recalled Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported June 12, 2026 · The recalled children's pajamas violate the mandatory flammability safety standard for children's sleepwear, posing a risk of serious burn injuries or death to... - Arctic Zone Titan Pro Coolers Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Imported by California Innovations and Sold at Costco
Consumer productReported June 12, 2026 · The recalled coolers' latch magnet can detach, posing risk of serious injury or death from a choking hazard. - 7-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.com by Hasuit Direct
Consumer productReported June 12, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Nimood Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported June 12, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails, because users can become entrapped within the bed rail or between the bed... - Kawasaki Motors USA Recalls Model Year 2026 Teryx4 H2 and Teryx5 H2 Recreational Off-Road Vehicles Due to Impact and Injury Hazards
Consumer productReported June 12, 2026 · The drive converter sheave can break in certain circumstances, resulting in metal fragments being discharged within the engine compartment and surrounding... - Hopelight Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by MOCCI SHOP
Consumer productReported June 12, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - Yamaha Recalls Model Year 2021-2022 Fleet Golf Cars Due to Risk of Serious Injury or Death from a Crash Hazard
Consumer productReported June 12, 2026 · The recalled golf cars' passenger-side brake cable could have been misrouted during assembly. If the cable was misrouted, abnormal wear can occur which can... - Timechee Changing Table 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 Timechee
Consumer productReported June 12, 2026 · The recalled dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that can result in a risk of serious injuries or death... - School Specialty Recalls Tip Restraint Kits Included in Childcraft Furniture Due to Risk of Serious Injury or Death from Tip-Over Hazard
Consumer productReported June 12, 2026 · The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards. Should the... - Merkury Innovations Recalls Hot + Cool Heating and Cooling Fans Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported June 12, 2026 · The fan can overheat, posing a risk of serious injury or death from a fire hazard. - LiKee Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by ChilanTech
Consumer productReported June 12, 2026 · The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach... - HSN Recalls Kitchen HQ Thermal Insulated Bowls Due to Fire Hazard
Consumer productReported June 12, 2026 · Metal springs in the detachable hinged lid of the insulated bowls can catch fire when used in the microwave, posing a fire hazard. - Joyin Recalls Sloosh Dive Sticks Due to Risk of Serious Injury from Impalement; Violate Federal Dive Sticks Ban
Consumer productReported June 12, 2026 · The recalled dive sticks violate the federal dive sticks ban because they exceeded the compress limit, posing an impalement hazard. In shallow water, children... - Vornado Air Recalls SRTH Small Room Tower Heaters Due to Fire Hazard
Consumer productReported June 5, 2026 · The recalled heater's fan blade can detach from the motor shaft, which can cause the fan to slow or stop, leading to overheating and melting of the enclosure... - SUNS International Recalls Residential Elevator Interlock Switches Due to Fall and Crushing Hazard; Risk of Death or Serious Injury
Consumer productReported June 5, 2026 · The affected interlock switches can become stuck in a retracted position, allowing the exterior door to remain unlocked, posing a risk of death or serious... - TOMY Recalls Boon NURSH 8 oz Reusable Baby Bottles Due to Choking Hazard; Sold at Walmart
Consumer productReported June 5, 2026 · The hard plastic outer shell can bubble or partially peel off, resulting in loose pieces of film-like plastic that pose a choking hazard to young children. - Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Broqixin
Consumer productReported June 5, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and...