Florida recalls
3,537 federal recalls affecting Florida in the last 12 months - 336 Florida-specific plus 3,201 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2025-10-29FDA-DeviceGE HealthcareClass IINationwideMaxicam; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
- 2025-10-29FDA-DeviceGE HealthcareClass IINationwideElscint Helix; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
- 2025-10-29FDA-DeviceGE HealthcareClass IINationwideElscint Varicam; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
- 2025-10-29FDA-DeviceGE HealthcareClass IINationwideElscint SPX6; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
- 2025-10-29FDA-DeviceGE HealthcareClass IINationwideElscint SPX4; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
- 2025-10-29FDA-DeviceGE HealthcareClass IINationwideElscint Model 4XX; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
- 2025-10-29FDA-DeviceGE HealthcareClass IINationwideElscint Cardial; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
- 2025-10-29FDA-DeviceHeartSineClass IINationwideHeartSine Pad-Pak, REF: PAD-PAK-01, PAD-PAK-02, PAD-PAK-03, PAD-PAK-04, PAD-PAK-07, PAD-PAK-03J, PAD-PAK-04J
Due to customer complaints, defibrillator pads may contain damage pins that disrupt the mechanical fit and electrical contact.
- 2025-10-29FDA-DeviceSedecalClass IINationwideFollow cleaning instructions for Sedecal X-ray equipment
Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD Veritor Connect Software recalled for unauthorized access risk
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD Phoenix M50 system recalled for unauthorized credential access
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD MAX System recalled for unauthorized credential access risk
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD BACTEC 9120 system recalled for credential access risk
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD BACTEC blood culture systems recalled for credential compromise
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
- 2025-10-29FDA-DeviceBecton DickinsonClass IINationwideBD EpiCenter system recalled for unauthorized credential access
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.
- 2025-10-29FDA-DeviceMedlineClass IINationwideMedline saline flush syringes recalled for concentration issue
Medline has identified a limited quantity of saline IV flush syringes that may not meet the required concentration of sodium chloride.
- 2025-10-29FDA-DeviceBaxterClass IINationwideWelch Allyn SureTemp Plus oral probe recalled for low temperature readings
Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower temperature than the true value, which may lead to a delay in managing fever-related symptoms or infection.
- 2025-10-29FDA-DeviceTandem Diabetes CareClass IINationwideTandem insulin pumps recalled for unexpected insulin dose risk
A software defect in versions 7.9.0.1 and 7.10.1 of the pump software for Tandem t:slim X2 and version 7.9.0.1 of the Tandem Mobi pump with Control-IQ+ technology that are paired with a G7 sensor may result in an unexpected automatic insulin correction bolus (autobolus ) which could result in hypoglycemia.
- 2025-10-29FDA-FoodTwin MarquisClass ITwin Marquis brand THICK SHANGHAI STYLE PLAIN NOODLE; NET WT 16 OZ; Ingredients: Bleached Wheat Flour, Water, Corn Starch, Salt, Sodium Benzoate (For Freshness); Contains: Wheat.; Produced on machinery that uses eggs; Manufactured by: Twin Marquis Inc. Brooklyn, NY 11206; UPC 7 60941 10301 6
Product contains undeclared egg, FD&C Yellow 5, and FD&C Yellow 6.
- 2025-10-29FDA-FoodMCI FoodsClass INationwideEgg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.50 oz; 72 count/case; UPC# 1 070657 497861 1
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
- 2025-10-29FDA-FoodMCI FoodsClass INationwideCheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 468334 8
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
- 2025-10-29FDA-FoodDemers FoodClass INationwideScott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
Contains Linguine manufactured by Nate's Fine Foods LLC recalled for Listeria monocytogenes and implicated in ongoing outbreak
- 2025-10-29FDA-FoodRolling Pin BakingClass IIRolling Pin brand Dubai Style Chocolate; 17.64 oz stand up pouch; Ingredients: Sugar, Cocoa Butter, Vegetable Fats, Whole Milk Powder, Pistachio (Tree Nut), Skimmed Milk Powder, Cocoa Mass, Kunefa, Soy Lecithin, Natural Vanilla Powder; Allergens: Contains Milk, Soy, Nuts (Pistachio), Gluten; Product of Belgium, Spain, USA, or Canada; Distributed & Imported by Rolling Pin Baking Company LLC; UPC # 642461215854
Product does not declare wheat in the allergen statement.
- 2025-10-29FDA-FoodGreat American Seafood ImportsClass IIGreat American branded Frozen raw shrimp skewer; 1lb bag UPC: 829944002716; 829944002372
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- 2025-10-29FDA-FoodGreat American Seafood ImportsClass IITovala branded Frozen raw phosphate free shrimp; 5oz IQF bag UPC: 829944085788
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- 2025-10-29FDA-FoodGreat American Seafood ImportsClass IIArctic Shores branded Frozen cooked salad shrimp; 6 oz bag UPC: 041130811685
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- 2025-10-29FDA-FoodGreat American Seafood ImportsClass IIArctic Shores; Best Yet; Great American; Master Catch branded Frozen Raw shrimp; 2lbs; 1lbs; UPC: 041130810923; 041512179471; 041130810978; 041130811029; 011110641182; 829944010636; 041130811333; 041130810916; 041130812460; 041130810824; 829944012463; 829944012012; 829944004079; 829944095060; 829944076984; 011110641168; 829944094537; 829944010612; 829944013583; 041512179471 011110643902; 041130811357;
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- 2025-10-29FDA-FoodGreat American Seafood ImportsClass IIArctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC: 041130810497; 041130810411; 041130811685; 041130810817; 042187002705; 829944012623; 042187002712; 829944012630; 042187002729; 829944011510; 041130812385; 042187002736; 042187002736; 829944013576; 829944012616; 829944093073; 041130810466; 041130810473; 042187002743; 829944011541; 717544137047; 829944012173; 829944002631; 042187002750; 829944011565; 829944010674; 829944011381; 04218700
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- 2025-10-29FDA-FoodGeorgia NutClass IINationwidetru fru Strawberries + Creme Freeze-Dried Fresh, retail pouch 3.4oz UPC 850048358249, 6 retail units per case
potential for metal in product
- 2025-10-29FDA-FoodGeorgia NutClass IINationwidetru fru Dark + White Chocolate Freeze-Dried Strawberries. 1.7oz retail pouch UPC 850048358331. 12 retail units per case. 3.4oz retail pouch UPC 850048358270. 6 retail units per case. 13oz retail pouch UPC 850048358379. 16 retail units per case.
potential for metal in product
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