Recalls in Massachusetts (page 39)
3965 recalls.
- 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. - 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. - Philips Tempus Pro Patient Monitor recall (Remote Diagnostic Technologies Ltd.)
Medical deviceClass IIReported January 14, 2026 · Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If... - 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 - 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. - 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. - Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK recall (Medline Industries, LP)
Medical deviceClass IIReported January 14, 2026 · Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient... - 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)... - The Pressio 2 ICP Monitoring System recall (Sophysa)
Medical deviceClass IIReported January 14, 2026 · Customer complaints of Pressio monitor rebooting. - Beckman Coulter UniCel Dxl 800 recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported January 14, 2026 · Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard... - Beckman Coulter UniCel Dxl 600 recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported January 14, 2026 · Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard... - 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. - The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with... recall (Roche Diagnostics Operations, Inc.)
Medical deviceClass IIReported January 14, 2026 · Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as... - Joyful Journeys Recalls Baby Loungers Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products
Consumer productReported January 9, 2026 · The recalled baby loungers violate the mandatory safety standard for Infant Sleep Products. The sides are too low to contain an infant and the enclosed... - PNW Components Recalls Aluminum Alloy Bicycle Pedals Due to Crash Hazard
Consumer productReported January 9, 2026 · The pedal axle can crack, causing the pedal to detach from the crank, posing a fall hazard to the rider. - Isla Rae Magnetic Wireless Chargers Recalled Due to Fire and Burn Hazards; Sold by TJX at T.J. Maxx and Marshalls Stores
Consumer productReported January 9, 2026 · The chargers can explode while in use, posing a fire and burn hazard. - Kori Gey Water Toy Kits Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Qaniy
Consumer productReported January 9, 2026 · The recalled toy kits violate the mandatory standard for toys containing button cell batteries because the compartment that holds the batteries can be easily... - RH Recalls Natural Antler Chandeliers Due to Impact Hazard
Consumer productReported January 9, 2026 · If the chandelier is hung at an angle on a vaulted ceiling or a sloped beam, the chandelier's canopy hardware can break, causing the chandelier to detach and... - Pounding Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard; Violate Mandatory Standard for Toys; Sold on Amazon by Findriver and Weeksome
Consumer productReported January 9, 2026 · The recalled pounding toys violate the mandatory standard for toys because they contain high-powered magnets, which can detach, posing an ingestion hazard to... - YOLAAH 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 January 9, 2026 · 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... - Vasicar 18-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported January 9, 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... - Sangohe Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported January 9, 2026 · 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... - Rattan 6-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 Rattan
Consumer productReported January 9, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in a risk of serious injuries... - NFSVLB Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning and Entrapment; Violate Mandatory Standard for Infant Bath Seats; Sold on Amazon by NFSVLB
Consumer productReported January 9, 2026 · The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, and have leg openings... - Marcus Adler Glove Recalls Julie and Judah Pajama Pants and Shorts Due to Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported January 9, 2026 · The pajama pants and shorts violate the mandatory standards for flammability of children's sleepwear, posing a risk of burn injuries to children. - The Kalencom Corporation Recalls SARO Braided Crib Bumpers Due to Risk of Serious Injury or Death from Suffocation; Violates Federal Crib Bumper Ban
Consumer productReported January 9, 2026 · The recalled padded crib bumpers violate the federal ban on crib bumpers because they can obstruct an infant's breathing, posing a risk of serious injury or... - Infant Innovations Recalls BabyBond Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures
Consumer productReported January 9, 2026 · The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the... - DR Power Equipment Reannounces and Expands Recall of Leaf Vacuums Due to Laceration Hazard; New Remedy Available
Consumer productReported January 9, 2026 · Pieces from the recalled leaf vacuums can come loose inside the unit, or debris can pierce the chute, resulting in material ejecting and posing a laceration... - Agrish Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Agrish Direct
Consumer productReported January 9, 2026 · 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... - 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. - 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... - Sheathes3D Seamless Viral Barrier recall (Sheathing Technologies Inc)
Medical deviceClass IIReported January 7, 2026 · Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk. - Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog... recall (Ferndale Laboratories, Inc.)
Medical deviceClass IIReported January 7, 2026 · Butyrate tube cracks during actuation, rendering product unusable. - Locatelli Pecorino Romano Cheese Grated recall (Wegmans Food Markets, Inc.)
FoodClass IReported December 31, 2025 · Product may be contaminated with Listeria monocytogenes. - Zen Cleanse Blend herbal tea recall (Bell Industries LLC)
FoodClass IIReported December 31, 2025 · Potential Salmonella contamination - 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... - BD Pyxis MedStation ES recall (CareFusion 303, Inc.)
Medical deviceClass IIReported December 31, 2025 · Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a... - Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz. recall (Silvestri Sweets Inc dba Carousel Candies)
FoodClass IReported December 31, 2025 · Undeclared pecan - Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pouch Bag. 5 oz. recall (Silvestri Sweets Inc dba Carousel Candies)
FoodClass IReported December 31, 2025 · Undeclared wheat - 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. - Restore Clinician Programmer Application recall (Medtronic Neuromodulation)
Medical deviceClass IIReported December 31, 2025 · Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume therapy, and... - 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. - LifeShield Drug Library Management recall (ICU Medical, Inc.)
Medical deviceClass IIReported December 31, 2025 · Software issue only allows Concentration Limits to be defined to one digit of precision past the decimal point (0.1) instead of three digits (0.001). If the... - LifeShield Drug Library Management recall (ICU Medical, Inc.)
Medical deviceClass IIReported December 31, 2025 · For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed. Users... - Brand Name: Alcon Laboratories recall (Alcon Research LLC)
Medical deviceClass IReported December 31, 2025 · Ophthalmic procedure packs may have incomplete seals affecting sterility. - Draeger Vapor 3000. Unheated recall (Draeger, Inc.)
Medical deviceClass IReported December 31, 2025 · A certain component of affected devices was not delivered within specification and contained impurities. - Draeger Vapor 2000. Unheated recall (Draeger, Inc.)
Medical deviceClass IReported December 31, 2025 · A certain component of affected devices was not delivered within specification and contained impurities. - Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common... recall (AGFA Healthcare Corp.)
Medical deviceClass IIReported December 31, 2025 · It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro exams. This can happen in case the framerate is increased on... - Celebration Herbals Senna Leaf Herbal Tea 24 Teabags recall (CELEBRATION HERBALS US)
FoodClass IIReported December 24, 2025 · possible salmonella - Chef brand Milk Pan 24cm recall (Shata Traders Inc.)
FoodClass IIReported December 24, 2025 · Products found to contain leachable lead levels (3.00 mg/L) - Intelerad InteleShare software recall (DICOM Grid, Inc.)
Medical deviceClass IIReported December 24, 2025 · Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing... - Ciclopirox Shampoo recall (SUN PHARMA /TARO)
DrugClass IIReported December 24, 2025 · Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Baclofen Tablets USP recall (Golden State Medical Supply Inc.)
DrugClass IIReported December 24, 2025 · Presence of Foreign Tablets/Capsules - BIOSURE HA SCREW recall (Smith & Nephew, Inc.)
Medical deviceClass IIReported December 24, 2025 · Removal of affected lot of screws due to labeling error. - Hardware configuration of the BeneVision Central Monitoring System recall (Mindray DS USA, Inc. dba Mindray North America)
Medical deviceClass IIReported December 24, 2025 · When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing. - GE Healthcare Carestation anesthesia system Power Management Board recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IReported December 24, 2025 · Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is... - GE Healthcare Carestation anesthesia system recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IReported December 24, 2025 · Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is... - GE Healthcare Carestation anesthesia system recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IReported December 24, 2025 · Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is... - 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...