Recalls in Arizona (page 22)
3972 recalls.
- a2 Platinum Premium infant formula Milk-based Powder with Iron 31.7oz recall (The a2 Milk Company)
FoodClass IReported June 10, 2026 · Possible contamination with Cereulide toxin. - Xyvona recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported June 10, 2026 · Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona - Xyvona recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported June 10, 2026 · Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona - Niacin Extended-release Tablets recall (Lannett Company Inc.)
DrugClass IIReported June 10, 2026 · Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint. - TopCare health recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - TopCare health recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - EQUALINE ultra strength recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - EQUALINE extra strength recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - GOODSENSE Ultra Strength recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - GOODSENSE Extra Strength recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - H.E.B Extra Strength Calcium Carbonate Antacid Tablets recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - HyVee recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - HyVee recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - Harris Teeter recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - FAMILY WELLNESS recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - FAMILY WELLNESS recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - DISCOUNT drug mart recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - CAREone recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - CAREone recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - MARKET BASKET ANTACID Calcium Carbonate 1000 mg recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - 24/7 life BY 7-ELEVEN recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - Extra strength Antacid Calcium Carbonate 750 mg recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - Good Neighbor Pharmacy recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - Good Neighbor Pharmacy recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - HALEON CALCIUM CARBONATE TUMS ANTACID recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - HALEON CALCIUM CARBONATE TUMS ANTACID recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - KIRKLAND Signature recall (Guardian Drug Co. Inc.)
DrugClass IIReported June 10, 2026 · Presence of foreign substance: small metallic particles in chewable tablets. - Amlodipine and Olmesartan Medoxomil Tablets recall (Ascend Laboratories, LLC)
DrugClass IIReported June 10, 2026 · Failed Dissolution Specifications: Olmesartan Medoxomil content below specifications - Duloxetine DR Capsules recall (Asclemed USA Inc.)
DrugClass IIReported June 10, 2026 · CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit. - Lidocaine HCl Injection USP recall (Spectra Medical Devices, Llc)
DrugClass IIReported June 10, 2026 · Lack of Assurance of Sterility - Lidocaine HCl Injection recall (Eugia US LLC)
DrugClass IIIReported June 10, 2026 · Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan - Sharpoint 2.2MM recall (SSC- Surgical Specialties Corporation)
Medical deviceClass IIReported June 10, 2026 · 3.0mm surgical knives labeled and packaged as 2.2mm surgical knives. - TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 ... recall (Grace Medical, Inc.)
Medical deviceClass IIReported June 10, 2026 · Due to incorrect functional length on device labeling. - Aligned Medical AMS16835 Fluids Kit RX recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported June 10, 2026 · Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits. - MAC 5 A4 Resting ECG Analysis System 855001-001 recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IIReported June 10, 2026 · Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with... - DeRoyal Industries Inc. Ref 46-406 recall (DeRoyal Industries Inc)
Medical deviceClass IIReported June 10, 2026 · Sterile wound dressing, lacks sterility assurance - BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis MedStation ES Tower REF: 352 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis Mini Main REF: 349 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis MedStation ES REF: 323 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis MedStation 4000 REF: 303 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - Phothera 200 recall (Daavlin Distributing Company)
Medical deviceClass IIReported June 10, 2026 · Some of the Calibration/Output Certificates had the outputs reversed. - Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus... recall (Advanced Bionics, LLC)
Medical deviceClass IIReported June 10, 2026 · Due to incorrect shelf-life expiration date. - Neptune Smart Docking Station recall (Stryker Corporation)
Medical deviceClass IIReported June 10, 2026 · It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required... - Covidien EndoStitch" Polysorb Single Use Loading Unit recall (Covidien, LP)
Medical deviceClass IIReported June 10, 2026 · The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure. - CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported June 10, 2026 · Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer... - Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description recall (B Braun Medical Inc)
Medical deviceClass IReported June 10, 2026 · These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary... - Spinocan Spinal Needle procedure kits: Material Description recall (B Braun Medical Inc)
Medical deviceClass IReported June 10, 2026 · These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary... - Spinal Needle procedure kits: Material Description recall (B Braun Medical Inc)
Medical deviceClass IReported June 10, 2026 · These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary... - The Large Volume Pump recall (Fresenius Kabi USA, LLC)
Medical deviceClass IIReported June 10, 2026 · Potential for the Cassette Loading Lever to break. - Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY ... recall (B Braun Medical Inc)
Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall... - Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 ... recall (B Braun Medical Inc)
Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall... - Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK RIVERSIDE HEALTH SYSTEM ... recall (B Braun Medical Inc)
Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall... - Brand Name: B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID... recall (B Braun Medical Inc)
Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall... - Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog... recall (B Braun Medical Inc)
Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall... - Brand Name: B. BRAUN MEDICAL INC. Product Name: NES1725KFXL SPINAL EPID CLOSED TIP... recall (B Braun Medical Inc)
Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall... - Brand Name: B. BRAUN MEDICAL INC. Product Name: BPSK recall (B Braun Medical Inc)
Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall... - Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY ... recall (B Braun Medical Inc)
Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall... - COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code:... recall (Covidien LLC)
Medical deviceClass IIReported June 10, 2026 · Due to customer complaint regarding incorrect display box labeling. - LVP software of the Ivenix Infusion System recall (Fresenius Kabi USA, LLC)
Medical deviceClass IReported June 10, 2026 · Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut... - Pediatric care bed recall (KAYSERBETTEN GMBH & CO. KG)
Medical deviceClass IReported June 10, 2026 · If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended... - 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... - Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by Gudook Outdoor Sports
Consumer productReported June 5, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation and certification... - Crenlux 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 Eicong
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... - Tiny Land Children's Play Tents Recalled Due to Risk of Injury from Irritation to Skin and Eyes
Consumer productReported June 5, 2026 · The recalled tents' fiberglass poles can shed fibers, posing an injury risk of skin and eye irritation. - Little Grape Land Recalls Nursing Pillows Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions
Consumer productReported June 5, 2026 · The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows and infant support... - Wyze Labs Recalls Solar Cam Pan Security Cameras Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported June 5, 2026 · The recalled Wyze Solar Cam Pan security cameras' incorrect assembly instructions can lead consumers to accidentally puncture the lithium ion battery's metal... - Fly By Jing recall (Fly By Jing Inc.)
FoodClass IIReported June 3, 2026 · Possible cross-contamination resulting in undeclared allergen ingredient (Peanut) - PRED MILD recall (AbbVie Inc.)
DrugClass IIIReported June 3, 2026 · Failed Stability Specifications - Nicotine Transdermal System Patch recall (AVEVA Drug Delivery Systems, Inc.)
DrugClass IIIReported June 3, 2026 · Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of... - Medline medical convenience kit labeled as EYE TRAY-LF recall (Medline Industries, LP)
Medical deviceClass IIReported June 3, 2026 · Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because... - Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 3, 2026 · It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of... - Azurion system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 3, 2026 · It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of... - Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation recall (Medtronic Neuromodulation)
Medical deviceClass IIReported June 3, 2026 · A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates. - Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation recall (Medtronic Neuromodulation)
Medical deviceClass IIReported June 3, 2026 · A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates. - HydroMARK Breast Biopsy Site Marker recall (Devicor Medical Products Inc)
Medical deviceClass IIReported June 3, 2026 · Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers. - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 recall (O&M HALYARD INC)
Medical deviceClass IIReported June 3, 2026 · Nitrile Exam Glove failed to meet specifications chemical permeation performance. - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported June 3, 2026 · A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns. These hardware updates... - Walmart Recalls Mainstays 9-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported May 28, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or... - Luminous Fidget Spinner Balls Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Anzmtosn
Consumer productReported May 28, 2026 · The recalled toys violate the mandatory safety standard for toys because the mini flashlight included with the fidget spinner balls contains button cell... - Missry Associates Recalls Misco Sports Light-Up Racket Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported May 28, 2026 · The racket sets violate the mandatory standard for toys because the screw on the racket used to secure the battery compartment does not remain attached when... - Joy Furniture Recalls Talan and Royce Living Room Furniture Sets Due to Risk of Serious Injury from a Fire Hazard
Consumer productReported May 28, 2026 · The power switch on the sofa, loveseat, or recliner can malfunction and overheat posing a risk of serious injury from a fire hazard. - Giantex Recalls Lounge Chairs Due to Amputation Hazard
Consumer productReported May 28, 2026 · Consumers can place their fingers in a pinch point, when adjusting the lounge chair, posing an amputation risk. - Tzumi Electronics Recalls SLF Sauna Blankets Due to Fire and Burn Hazards
Consumer productReported May 28, 2026 · The recalled sauna blankets can overheat, posing fire and burn hazards. - Lithium Coin Batteries Recalled Due to Battery Ingestion; Violates Federal Statute for Child-Resistant Packaging of Coin Batteries; Imported by Proudly American Store, of Canada
Consumer productReported May 28, 2026 · The recalled coin batteries are not in child-resistant packaging and do not bear the warning labels required under Reese's Law. When button cell or coin... - Daoen Recalls Zen Magnetic Promotional Ball Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
Consumer productReported May 28, 2026 · The recalled magnetic balls violate the mandatory standard for toys because they are loose high-powered magnets, posing an ingestion hazard to children. When... - MiniWarGaming and Primal Horizon Disc Magnets Recalled Due to Risk of Serious Injury or Death from Ingestion; Violate Mandatory Standard for Magnets; Imported by MiniWarGaming
Consumer productReported May 28, 2026 · The magnets violate the mandatory safety standard for magnets because the high-powered magnets fit within CPSC's small parts cylinder and are stronger than...