Recalls in Virginia (page 20)
4022 recalls.
- Medline convenience kits: BREAST-HERNIA-PORT CDS-LF CDS984853L recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716 recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline EBSI Kit EBSI1534 recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported June 24, 2026 · Potential software error in the Automated Impella Controller ("AIC" ) when used in conjunction with left ventricular Impella devices. - 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... - Individual Unit Label recall (Kettle Cuisine, LLC)
FoodClass IReported June 17, 2026 · Contains undeclared allergen (shrimp). - Merlin" Patient Care System recall (Abbott Medical)
Medical deviceClass IIReported June 17, 2026 · Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to... - NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product... recall (In2bones USA, LLC)
Medical deviceClass IIReported June 17, 2026 · Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label. - Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE recall (HF Acquisition Co LLC)
Medical deviceClass IIReported June 17, 2026 · Due to incorrect incubation process being performed on product. - Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE recall (HF Acquisition Co LLC)
Medical deviceClass IIReported June 17, 2026 · Due to incorrect incubation process being performed on product. - CGuard¿ Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - CGuard Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - Brand Name: CGuard Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - CGuard Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - Brand Name: CGuard¿ Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - Brand Name: CGuard¿ Prime Carotid Stent System recall (INSPIREMD Inc)
Medical deviceClass IIReported June 17, 2026 · Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent. - 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. - NEURO NOURISH dietary supplement recall (SENSORY SUPPLEMENT LLC)
FoodClass IIReported June 17, 2026 · Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste. - 1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules recall (Total Nutrition Inc)
FoodClass IReported June 17, 2026 · Product may be contaminated with Salmonella. - Park St. Deli Macaroni & Cheese recall (BEF Foods, Inc)
FoodClass IIReported June 17, 2026 · Undeclared allergen (soy lecithin). - BEEKEEPER'S NATURALS Saline Nasal Spray recall (BEEKEEPER'S NATURALS USA INC.)
DrugClass IReported June 17, 2026 · Microbial Contamination of Non-Sterile Products - Budesonide Inhalation Suspension recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported June 17, 2026 · Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the... - 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. - Zep recall (Zep Inc)
DrugClass IIReported June 17, 2026 · Microbial contamination of sterile products - 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 - Epinephrine Injection recall (Fresenius Kabi USA, LLC)
DrugClass IIIReported June 17, 2026 · Failed Impurities/Degradations Specifications - DOXOrubin Hydrochloride Liposome injection recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IReported June 17, 2026 · Presence of Particulate matter: Particulate matter identified as glass. - Orca Single Use Air/Water and Suction Valves recall (Boston Scientific Corporation)
Medical deviceClass IIReported June 17, 2026 · Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence... - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - MOSAIQ Oncology Information System recall (Elekta, Inc.)
Medical deviceClass IIReported June 17, 2026 · Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs. - Boston Scientific Model SC-4318 recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported June 17, 2026 · Sterile anchors my lack sterility assurance. - Boston Scientific TCN Electrodes: REF: TCN-5 recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported June 17, 2026 · Reusable electrodes may not meet expected performance levels. - Boston Scientific CSK Electrodes: REF: CSK-TC10 recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported June 17, 2026 · Reusable electrodes may not meet expected performance levels. - Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit recall (Inter-Med Llc)
Medical deviceClass IIReported June 17, 2026 · Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different... - Hintermann Series Talar Implant recall (DT MedTech, LLC)
Medical deviceClass IIReported June 17, 2026 · Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant... - Siemens Dimension Tacrolimus Flex Reagent Cartridge recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported June 17, 2026 · A potential positive bias in quality control (QC) and patient sample results in three lots of the Dimension Tacrolimus (TAC) Flex reagent cartridge. - Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number:... recall (The Binding Site Group, Ltd.)
Medical deviceClass IIReported June 17, 2026 · It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being... - Medartis APTUS recall (Medartis AG)
Medical deviceClass IIReported June 17, 2026 · The cannulation of the CCS screw is not centered. - NexxZr T Multi A3.5 W98-16mm recall (Sagemax Bioceramics, Inc.)
Medical deviceClass IIReported June 17, 2026 · Yttrium-stabilized zirconium oxide discs for fixed all-ceramic dental restorations may have reduced or missing dentin layer and when used clinically in the... - SD LTM 64 PLUS recall (Micromed S.p.A.)
Medical deviceClass IIReported June 17, 2026 · Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple... - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW ... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number:... recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320 recall (Avanos Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - Bicarby" Dialysate recall (Fresenius Medical Care Holdings, Inc.)
Medical deviceClass IIReported June 17, 2026 · Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the... - EXCOR Pediatric Ventricular Assist Device recall (BERLIN HEART GMBH)
Medical deviceClass IIReported June 17, 2026 · Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures. - Mahurkar Elite PASS Trays recall (Mozarc Medical US LLC)
Medical deviceClass IIReported June 17, 2026 · The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays. - Allia Moveo angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 7 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 5 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 3 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Plum Duo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Plum Duo Infusion Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Plum Solo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - 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...