Recalls in Florida (page 10)
4115 recalls.
- Truststone Group Recalls XO Poppy Power Trip Magnetic Wireless Power Banks Due to Fire and Burn Hazards; Sold Exclusively at TJX and Marshalls Stores
Consumer productReported September 3, 2026 · The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers. - Skip Hop Recalls Baby Sesame Street Elmo Silicone Teethers Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported September 3, 2026 · The black eyes can detach from the recalled teether if frozen, posing a risk of serious injury or death from a choking hazard. - GIHNJSI Squeezy Dumplings Toys Recalled Due to Serious Ingestion, Choking and Obstruction Hazards; Sold on Amazon by Chenyuanhui
Consumer productReported September 3, 2026 · The squeezy toys contain water beads. If ingested, water beads expand and can pose deadly ingestion, choking, and intestinal obstruction hazards inside a... - OKK Trading Recalls Rainbow Mystery Squishy Bun Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 3, 2026 · The squishy bun toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly... - Gizoon Direct Recalls Six-Drawer Double Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported September 3, 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... - Branch Recalls Ergonomic Chairs Due to Fall Hazard
Consumer productReported September 3, 2026 · The backrests of the chairs can detach, posing a fall hazard to consumers. - Daikin Comfort Technologies Manufacturing Recalls Amana Through-The-Wall Air Conditioners and Heat Pumps Due to Risk of Serious Injury from Fire
Consumer productReported September 3, 2026 · The snubber circuit can emit flames if it shorts, posing a risk of serious injury due to fire hazard. - 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 Loyoda Direct and Loyoda
Consumer productReported September 3, 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... - SHEIN Distribution Corporation Recalls Spiral Toys Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Ball Ban
Consumer productReported September 3, 2026 · The toys violate the small ball ban because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard. - Audio Partnership Recalls Cambridge Audio Yoyo (M) Portable Bluetooth Speakers Due to Fire Hazard
Consumer productReported September 3, 2026 · The lithium-ion batteries in the Cambridge Audio Yoyo (M) Portable Bluetooth Speaker can overheat, posing a fire hazard. - Nanjing Wu Hai Smart Home Appliance Store Recalls Alanca 6-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Consumer productReported September 3, 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... - Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - bettergoods brand Pistachio Nut Butter recall (Botticelli Foods, LLC)
FoodClass IReported September 2, 2026 · Product may be contaminated with Salmonella. - Outshine Fruit Bars Strawberry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Black Cherry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Tangerine recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Grape recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bar Watermelon recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Strawberry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - POWERSEAL 5 MM recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 2, 2026 · Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device. - Medline convenience kits labeled as: 1) LAMI FUSION recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) LAVH recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) C-SECTION recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) GYN ROBOTIC CDS recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) MAJOR GYN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: LTP CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) MAJOR PROCEDURE recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: MAJOR HEAD AND NECK PPS recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) OPEN HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) FEMORAL PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Merge PACS and Merge OrthoPACS recall (Merge Healthcare, Inc.)
Medical deviceClass IIReported September 2, 2026 · Software issue may cause measurements to be displayed inaccurately. - Horizon Organic ORG ASEP CHOC MILK 1% 8OZ 12 CT recall (Horizon Organic Dairy, LLC)
FoodClass IIReported September 2, 2026 · Product has the potential to be spoiled. - Lactated Ringer's Injection USP recall (B BRAUN MEDICAL INC)
DrugClass IReported September 2, 2026 · Presence of Particulate matter. - Ramipril Capsules USP recall (Hikma Pharmaceuticals USA INC.)
DrugClass IIReported September 2, 2026 · Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU). - Tyenne recall (Fresenius Kabi USA, LLC)
DrugClass IReported September 2, 2026 · Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles. - Paxil CR recall (Apotex Corp.)
DrugClass IIReported September 2, 2026 · Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria - Acthar Gel recall (Mallinckrodt Hospital Products Inc.)
DrugClass IIReported September 2, 2026 · Presence of particulate matter: glass and stopper piece - Zicam recall (Church & Dwight Co., Inc.)
DrugClass IIReported September 2, 2026 · CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing - Clobetasol Propionate Cream USP recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported September 2, 2026 · Failed content uniformity specifications. - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - ORT300 recall (IMRIS Imaging Inc)
Medical deviceClass IIReported September 2, 2026 · The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and... - ORT200 recall (IMRIS Imaging Inc)
Medical deviceClass IIReported September 2, 2026 · The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and... - healthmark ProChek-W Protein Test for Robotic Arms recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported September 2, 2026 · Test manufactured with an expired ingredient which may present as either a false negative or positive. - healthmark ProChek-II recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported September 2, 2026 · Test manufactured with an expired ingredient which may present as either a false negative or positive. - FUJIFILM Synapse PACS software v7.4.310 recall (FUJIFILM Healthcare Americas Corporation)
Medical deviceClass IIReported September 2, 2026 · Software issue may cause the ruler measurement to be inaccurate. - CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B... recall (ConMed Corporation)
Medical deviceClass IIReported September 2, 2026 · Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability. - Fresenius Medical Care recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 2, 2026 · Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ ... - Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm recall (Henry Schein Inc.)
Medical deviceClass IIReported September 2, 2026 · Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device. - Structur 2 SC Temporary Resin Cartridge Refill 75Gm recall (Henry Schein Inc.)
Medical deviceClass IIReported September 2, 2026 · Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device. - Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital... recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported September 2, 2026 · Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose. - Midmark Digital ECG HD+12 recall (Midmark Corporation)
Medical deviceClass IIReported September 2, 2026 · A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation. - Midmark IQecg Digital ECG recall (Midmark Corporation)
Medical deviceClass IIReported September 2, 2026 · A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY... recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - American Contract System Convenience Kit recall (American Contract Systems Inc)
Medical deviceClass IIReported September 2, 2026 · The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has... - American Contract System Convenience Kits recall (American Contract Systems Inc)
Medical deviceClass IIReported September 2, 2026 · The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has... - American Contract System Convenience Kit recall (American Contract Systems Inc)
Medical deviceClass IIReported September 2, 2026 · The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has... - American Contract System Convenience Kit recall (American Contract Systems Inc)
Medical deviceClass IIReported September 2, 2026 · The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has... - Medline medical convenience kit labeled as: TRACH TUBE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Component labeling discrepancy - Onli 17cm Hydrophilic Urethral Intermittent Catheter recall (Hollister Ulc)
Medical deviceClass IIReported September 2, 2026 · Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential... - Medline breathing circuits labeled as: 1) MEDLINE HUDSON RCI recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit... - Medline breathing circuits labeled as: 1) HUDSON RCI recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit... - Medline Hudson RCI recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit... - Philips Incisive CT with software V4.5&V5.0 recall (Philips Healthcare (Suzhou) Co., Ltd.)
Medical deviceClass IIReported September 2, 2026 · Potential of failing to trigger clinical scan during Bolus Tracking. - Montessori Baby Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Chillife Official
Consumer productReported August 27, 2026 · The recalled baby toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and longer... - Walmart Reannounces Recall of Mainstays Nine-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Walmart Distributed Recalled Dressers Post-Recall; Sold to Consumers Through Liquidators
Consumer productReported August 27, 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... - Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by YERYORK
Consumer productReported August 27, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of injury or... - Little Loves & Co. Recalls Youth Clothing with Drawstrings Due to Risk of Serious Injury or Death from Entrapment Hazard
Consumer productReported August 27, 2026 · The drawstrings in the recalled clothing can get caught on objects and cause death or serious injury to children due to an entrapment hazard. - Steelite Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by Longer 3D
Consumer productReported August 27, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing a risk of serious injury or... - Excel Industries Recalls Accessory LED Light Kits Due to Risk of Serious Injury from Fire Hazard
Consumer productReported August 27, 2026 · The light bars can overheat or produce flames, posing a risk of serious injury from a fire hazard. - Kmaier Recalls Infant Walkers Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers
Consumer productReported August 27, 2026 · The recalled walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step... - AudioLineOut Recalls Studio Six Headphone Amplifiers Due to Risk of Serious Injury or Death from Electrocution Hazard
Consumer productReported August 27, 2026 · When the amplifiers are used with aftermarket metal base tubes, the bare metal can become electrified, posing a risk of serious injury or death from... - HABA USA Recalls Rainbow Rattle Grasping and Teething Toys Due to Risk of Serious Injury or Death from Choking and Ingestion Hazards
Consumer productReported August 27, 2026 · The glued knot on the elastic cord can become untied on the recalled product, allowing young children access to the small wooden and plastic pieces, posing a... - Diamond Wipes International Recalls MD Wipe Outz Numbing Tattoo Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Consumer productReported August 27, 2026 · The recalled numbing wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of... - Conair Expands Recall of Cuisinart Grill Brushes Due to Ingestion Hazard; Over 3.6 Million Brushes Now Recalled
Consumer productReported August 27, 2026 · Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that... - Organic Whole Mixed Berries recall (Publix Super Markets, Inc.)
FoodClass IReported August 26, 2026 · Due to potential E. coli O145:H28 contamination - Organic Whole Mixed Berries recall (Publix Super Markets, Inc.)
FoodClass IReported August 26, 2026 · Due to potential E. coli O145:H28 contamination