Recalls in Florida (page 7)
4115 recalls.
- MR 5300 Model Number recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Name recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Ingenia Elition S and Ingenia Elition X recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Ingenia 3.0T and Ingenia 3.0T CX recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Ingenia Ambition S and Ingenia Ambition X recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Ingenia 1.5T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Evolution upgrade 1.5T and Evolution upgrade 3.0T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Achieva XR recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Achieva 3.0T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Achieva 1.5T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS... recall (Medline Industries, LP)
Medical deviceClass IIReported September 30, 2026 · Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush.... - Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK... recall (Medline Industries, LP)
Medical deviceClass IIReported September 30, 2026 · Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush.... - CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 30, 2026 · Communication to recommend reviewing the IFU and ensuring that all treatment preparation and handling steps are performed as instructed. - PowerLED 300 Concealed Lighting System recall (Maquet SAS)
Medical deviceClass IIReported September 30, 2026 · The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury. - Midmark IQvitals Zone recall (Midmark Corporation)
Medical deviceClass IIReported September 30, 2026 · A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used. - Midmark IQvitals Zone recall (Midmark Corporation)
Medical deviceClass IIReported September 30, 2026 · A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used. - Midmark IQvitals Zone recall (Midmark Corporation)
Medical deviceClass IIReported September 30, 2026 · A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used. - Midmark IQvitals Zone recall (Midmark Corporation)
Medical deviceClass IIReported September 30, 2026 · A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used. - Brand Name: Heidelberg Engineering GmbH Product Name: SPECTRALIS with Flex Module ... recall (Heidelberg Engineering GmbH)
Medical deviceClass IIReported September 30, 2026 · Wheels may come loose when module is being pushed or pulled during movement or transportation, affecting stability of the stand. The stand may tip over as a... - Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5 recall (Boston Scientific Corporation)
Medical deviceClass IReported September 30, 2026 · Tip may fracture or detach, leading to device fragments remaining within the patient or migrating through the vasculature. Patient impact may include prolonged... - Halyard IV START KIT NON-STERILE recall (AVID Medical, Inc.)
Medical deviceClass IReported September 30, 2026 · Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides. - ABC Trading Recalls Light-Up Children’s Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 24, 2026 · The recalled children’s toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries... - Love To Dream Recalls Portable Sleep Machines Due to Risk of Injury from Fire and Burn Hazards
Consumer productReported September 24, 2026 · The lithium-ion battery in the recalled portable sleep machines can overheat if the charger is not compatible with the unit, posing a risk of injury from fire... - INMO International Technology Limited Recalls INMO Air3 Smart Glasses Due to Risk of Serious Injury or Death from Burn Hazard
Consumer productReported September 24, 2026 · The left temple of the recalled smart glasses can overheat during extended use, posing a risk of serious injury or death due to burn hazard. - Style Homeware Recalls Emerspring Mattresses Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability
Consumer productReported September 24, 2026 · The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire. - Yuyitop Recalls Aitjunz 8-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 24, 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... - Xinan Home Recalls WinxMatrs Mattresses Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability
Consumer productReported September 24, 2026 · The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire. - NEWDERY Power Banks Recalled Due to Fire and Burn Hazards; Risk of Serious Injury; Sold on Amazon
Consumer productReported September 24, 2026 · The lithium-ion battery in the power banks can explode or ignite, posing fire and burn hazards to consumers. - The Blue Cactus Company Reclining Chair Battery Packs Recalled Due to Fire and Burn Hazards; Sold on Amazon
Consumer productReported September 24, 2026 · The lithium-ion battery in the recalled battery packs can overheat, posing fire and burn hazards to consumers. - Hyperfuels Recalls Methanol and Ethanol Fuel Containers Due to Risk of Serious Injury or Death from Child Poisoning and Flame Jetting; Violates Multiple Federal Safety Standards
Consumer productReported September 24, 2026 · The recalled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under... - 5Color Recalls Children’s Bicycle Helmet and Pads Sets Due to Risk of Serious Injury or Death from Head Injury; Violate Mandatory Standard for Bicycle Helmets
Consumer productReported September 24, 2026 · The helmets in the recalled sets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation... - ZCK01 Recalls Kesyup Mattresses Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability
Consumer productReported September 24, 2026 · The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire. - Mon Sire Brie recall (Optimus Inc. d/b/a/ Markys Caviar)
FoodClass IReported September 23, 2026 · The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes. - Hexing Haw Balls candy recall (Tiffany Food Corp)
FoodClass IIIReported September 23, 2026 · Unapproved dye Ponceau 4R - PUMPKIN SPICE NO BAKE COOKIE recall (Best Friends Bakery, LLC)
FoodClass IIReported September 23, 2026 · Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain... - BH Bold Chef Salad Kit. Ingredients: Iceberg Lettuce recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Pico De Gallo. Ingredients: Tomato recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Fresh Pico Tray. Ingredients: Tomato recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Pico De Gallo Hot. Ingredients: Tomato recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Tomato Salsa Fresca. Ingredients: Tomatoes recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Salsa Fresca Medium. Ingredients: Tomato recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Salsa Verde Mild. Ingredients: Whole Tomatillos recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Salsa Roja Medium. Ingredients: Fire Roasted Diced Tomatoes in Juice recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Pico De Gallo Spicy. Ingredients: Tomato recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Pico De Gallo Mild. Ingredients: Tomato recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Hot Pico De Gallo. Ingredients: Tomatoes recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Mild Pico De Gallo. Ingredients: Tomatoes recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Pico De Gallo. Ingredients: Tomato recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Pico De Gallo. Ingredients: Tomato recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Pineapple Mango Salsa Mild. Ingredients: Mango recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Mango Pico De Gallo. Ingredients: Mango recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Authentic Guacamole. Ingredients: Guacamole recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Spicy Guacamole. Ingredients: Guacamole recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Fiesta Salad with Shrimp. Ingredients: Salad recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Taco Dip. Ingredients: Refried Vegetarian Beans *** Guacamole recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Spicy Pimento Cheese Dip. Ingredients: Sharp Cheddar Cheese *** Cream Cheese ***... recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Spicy Jalapeno Jarlsberg Dip. Ingredients: Mayonnaise *** Jarlsberg Cheese *** Red Onion recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Spicy Roast Beef Sandwich recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Rice & Bean Burrito. Ingredients: Rice recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - Diced Jalapenos. Ingredients: Jalapeno Pepper. Net Wt: 3.75 oz. Keep Refrigerated. ... recall (Taylor Fresh Foods Inc)
FoodClass IReported September 23, 2026 · Potential contamination with Salmonella. - CADD Yellow Medication Cassette Reservoir with NRFit connector US Product Codes:... recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Reservoirs may exhibit medication leakage at the joint between luer connector and tubing. Issue could result in delay or interruption of therapy, under... - Convenience kits CATARACT PACK DYNJ59881A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Boston Scientific Corporation StoneSmart Connect Console Contents: recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 23, 2026 · A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power... - REF:B5ST Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - REF:B5LT Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - REF:B12LT Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - REF:B11LT Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - REF:2B5ST Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - REF:2B5LT Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - Kinos Axiom Total Ankle System with Axiom PSR recall (restor3d Inc.)
Medical deviceClass IIReported September 23, 2026 · Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard... - Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT... recall (Wilson-Cook Medical Inc.)
Medical deviceClass IIReported September 23, 2026 · Due to issue with endoscope adherence and inability to spray powder. Firm will provide an updated Instruction for Use (IFU). - Happiest Baby recall (Happiest Baby, Inc)
Medical deviceClass IIReported September 23, 2026 · Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA. - Happiest Baby recall (Happiest Baby, Inc)
Medical deviceClass IIReported September 23, 2026 · Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA. - GM Helix Implant recall (Straumann USA LLC)
Medical deviceClass IIReported September 23, 2026 · There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside. - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Oncology sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Oncology sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Non-Dedicated Gravity Administration Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Plum administration sets recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Philips PIC iX Essentials REF:867093 recall (Philips North America)
Medical deviceClass IIReported September 23, 2026 · Due to software malfunction, patient information system may freeze and become unresponsive. - Philips Patient Information Center iX REF:866389 recall (Philips North America)
Medical deviceClass IIReported September 23, 2026 · Due to software malfunction, patient information system may freeze and become unresponsive. - BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump... recall (BD SWITZERLAND SARL)
Medical deviceClass IReported September 23, 2026 · Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance. - DuoGlide Short-Term Straight Dialysis Catheter recall (Bard Access Systems, Inc.)
Medical deviceClass IReported September 23, 2026 · this is a downstream recall of class I recall RES 98777 - Power-Trialysis Short-Term Straight Dialysis Catheter recall (Bard Access Systems, Inc.)
Medical deviceClass IReported September 23, 2026 · this is a downstream recall of class I recall RES 98777 - Foods Alive organic moringa leaf powder recall (FOODS ALIVE INC.)
FoodClass IReported September 23, 2026 · Potential Salmonella contamination - Thyroid Tablets recall (VITRUVIAS THERAPEUTICS INC)
DrugClass IReported September 23, 2026 · Superpotent Drug - Dopamine HCl Inj. recall (Pfizer)
DrugClass IIReported September 23, 2026 · Lack of Assurance of Sterility - Chlorthalidone Tablets recall (Inventia Healthcare Limited)
DrugClass IIReported September 23, 2026 · Failed Dissolution Specifications - Lidocaine Ointment USP recall (SUN PHARMA /TARO)
DrugClass IIReported September 23, 2026 · Failed Content Uniformity Specifications. Out of Specification for Assay during analysis at the 24- month long term stability station, at (25¿C,60%RH). - Fluphenazine HCl Elixir recall (Safecor Health, LLC)
DrugClass IIReported September 23, 2026 · Failed Stability Specifications - Fluphenazine HCl Elixir recall (Safecor Health, LLC)
DrugClass IIReported September 23, 2026 · Failed Stability Specifications - Fluphenazine HCl Elixir recall (Safecor Health, LLC)
DrugClass IIReported September 23, 2026 · Failed Stability Specifications - Fluphenazine HCl Elixir recall (Safecor Health, LLC)
DrugClass IIReported September 23, 2026 · Failed Stability Specifications - Fluphenazine HCl Elixir recall (Safecor Health, LLC)
DrugClass IIReported September 23, 2026 · Failed Stability Specifications