State

Florida product recalls

73,187 recalls have nationwide distribution and so reach Florida. 12,855 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total: 12,855
Critical: 1,775
Severe: 2,991
Most recent: 2026-10-02

Of the 12,855 recalls naming Florida we have scored against our rubric, 1,775 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,991 (23%) are Severe.

Which agencies issued them

These figures cover only the 12,855 recalls whose distribution notice names Florida specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12301–12325 of 86042

HighFDA (Food)·F-1289-2024·2024-06-12
Cream Cheese Spread Recalled Due to Potential Salmonella Contamination
Schreiber Foods is recalling cream cheese spread sold under Dunkin, Happy Farms, Hy-Vee, Piggly Wiggly, and Schnucks brands due to potential Salmonella contamination. The recalled products were distributed to multiple states and Puerto Rico.
Product
Cream Cheese Spread. Keep Refrigerated, packaged under the following brands: 1. Dunkin, Net Wt 8 oz. (226g), UPC 0 29244-01497 0. Manufactured Exclusively for Dunkin Brands Inc. 130 Royal St. Canton, MA 02021 2. Happy Farms, Net Wt 8 oz. (226g). UPC 4099100101737, Dist…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-1938-2024·2024-06-12
Medline Luer Slip Syringes Recalled for Inaccurate Volume Delivery
Medline Industries is recalling over 5 million Luer Slip disposable syringes because testing documentation does not confirm they deliver accurate volumes across their claimed capacity range. This poses a risk to patient health.
Product
MEDLINE LUER SLIP DISPOSABLE SYRINGE WITHOUT NEEDLE, REF SYR101020
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1959-2024·2024-06-12
ADVANTA VXT Vascular Graft Recalled for Slider Rod Separation
The ADVANTA VXT vascular graft is being recalled because its slider rod can separate from the swivel core, creating a gap between components. No injuries have been reported.
Product
ADVANTA VXT, 6X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1971-2024·2024-06-12
ADVANTA VXT Vascular Grafts Recalled for Slider Rod Separation
Atrium Medical is recalling 53,308 ADVANTA VXT vascular grafts worldwide due to reported separation of the slider rod from the swivel core, with a gap observed between the components.
Product
ADVANTA VXT, 6X80, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1966-2024·2024-06-12
ADVANTA VXT Vascular Graft Slider Component Separation Recall
Atrium Medical Corporation is recalling its ADVANTA VXT vascular graft due to reports that the Slider GDS Swivel Rod can separate from the Swivel Core, creating a gap between components.
Product
ADVANTA VXT, 7X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2016-2024·2024-06-12
FLIXENE Vascular Graft Recalled for Slider Component Separation
Atrium Medical is recalling the FLIXENE vascular graft due to reported separation of the Slider GDS Swivel Rod from its core. Component separation could affect graft function.
Product
FLIXENE, 4-6X45, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1949-2024·2024-06-12
Medical device recall: HA FlexTrak patient transport trolley oil leak hazard
Philips is recalling the HA FlexTrak patient transport trolley due to potential oil leaks from the hydraulic system that create slipping and falling hazards. Approximately 100 units have been distributed worldwide.
Product
HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710006412
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1982-2024·2024-06-12
Vascular Graft Component Separation Risk in ADVANTA VXT Grafts
ADVANTA VXT vascular grafts are being recalled due to reported separation of the Slider GDS Swivel Rod from its core. This mechanical failure could compromise graft function.
Product
ADVANTA VXT, 8X40, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1301-2024·2024-06-12
Panera Oatmeal Raisin with Berries Cookies Recalled for Potential Salmonella
Rise Baking Company is recalling approximately 29,019 cases of Panera Oatmeal Raisin with Berries Cookie dough pucks due to potential Salmonella contamination. The affected products were distributed across 20 states.
Product
Panera Oatmeal Raisin with Berries Cookie, Net Wt. 41.25 lb (18.71kg), 220/3 oz cookie dough pucks/case
Category
Food
Distribution
21 states
HighFDA (Devices)·Z-1944-2024·2024-06-12
Alaris Pump Infusion Set Drip Chamber May Detach During Use
A defective drip chamber in the Alaris Pump Infusion Set may detach from the tubing, potentially delaying treatment or causing unintended exposure to medications. BD is recalling approximately 11,300 units distributed across the US and Canada.
Product
Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set used for delivery of fluids, medication, blood and blood products.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2015-2024·2024-06-12
FLIXENE Vascular Graft Slider Rod Separation Defect Recall
Atrium Medical Corporation has recalled FLIXENE vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core and a notable gap between the pieces.
Product
FLIXENE, 4-7X45, 2GDS, GWT. Double-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1964-2024·2024-06-12
Vascular Graft Component Separation Recall from Atrium Medical
Atrium Medical is recalling 53,308 ADVANTA VXT vascular grafts due to reports of Slider GDS Swivel Rod separation from the Swivel Core. Component separation could compromise device function.
Product
ADVANTA VXT, 5X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1958-2024·2024-06-12
Vascular graft slider component separation poses implant failure risk
Atrium Medical is recalling ADVANTA VXT vascular grafts due to separation of the slider swivel rod from its core. This structural defect could lead to device failure. Over 53,000 units are affected worldwide.
Product
ADVANTA VXT, 5X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1980-2024·2024-06-12
Vascular Graft Recall for Component Separation in ADVANTA VXT
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. This component separation could compromise device function.
Product
ADVANTA VXT, 6X80, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2010-2024·2024-06-12
Vascular Graft Device Recalled for Slider Rod Separation Risk
Atrium Medical Corporation is recalling approximately 53,308 FLIXENE vascular graft units worldwide due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, creating gaps that could affect device performance.
Product
FLIXENE, 7X50, 1GDS, STR. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2024-2024·2024-06-12
Medline Sterile Iris Scissors Recall Due to Detachable Tip Protector
Medline is recalling 67,811 units of sterile iris scissors because the tip protector may detach during use. The recall affects units distributed nationwide and internationally.
Product
MEDLINE STERILE IRIS SCISSORS CVD/STD REF DYNJ04049 (case) and DYNJ04049H (individual unit)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1954-2024·2024-06-12
ADVANTA VXT vascular graft recalled for slider rod separation
Atrium Medical is recalling ADVANTA VXT vascular grafts due to complaints of separation between the slider rod and swivel core, which could affect proper device function.
Product
ADVANTA VXT, 5X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1290-2024·2024-06-12
Whipped Cream Cheese Spread Recalled for Potential Salmonella Contamination
Schreiber Foods Inc is recalling whipped cream cheese spread sold under multiple store brands due to potential Salmonella contamination. Consumers should return the product to the retailer.
Product
Whipped Cream Cheese Spread. Net Wt 8 oz. (226g) Keep Refrigerated, packaged under the following brands: 1. Dutch Farms, Net, UPC 0 919145-67990 1. Distribured By: Dutch Farms, Chicago, IL 60628. 2. Fareway, UPC 0 21333-83051 5. Packed for Fareway Store, Inc. Boone…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-2027-2024·2024-06-12
GE HealthCare CRITIKON ONE-CUF blood pressure cuffs may give inaccurate readings
GE HealthCare CRITIKON ONE-CUF blood pressure cuffs may provide inaccurate measurements. The FDA recalls approximately 23,180 boxes distributed across 20 US states.
Product
GE HealthCare CRITIKON ONE-CUF blood pressure cuffs, Model numbers: 1. ONE-A1-1B, ONE-CUF, SMALL ADULT, 1 TB BAYONET, 17 - 25 CM, 20/BOX; 2. ONE-A1-2A, ONE-CUF, SMALL ADULT, DINACLICK 80369-5, 17 - 25 CM, 20/BOX; 3. ONE-A2-1B, ONE-CUF, ADULT, 1 TB BAYONET, 23 - 33 CM…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0532-2024·2024-06-12
Prescription Rizatriptan Benzoate Tablets Recalled for Chemical Impurity
Glenmark Pharmaceuticals recalls Rizatriptan Benzoate 5mg tablets due to excess N-Nitroso Desmethyl Rizatriptan impurity. The nationwide recall affects 3,480 cartons with lots 19233788 and 19224445.
Product
RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1974-2024·2024-06-12
Vascular graft component separation in Atrium Medical ADVANTA VXT devices
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts worldwide due to reports of separation between the swivel rod and swivel core. The component failure could affect graft function.
Product
ADVANTA VXT, 8X40, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1988-2024·2024-06-12
Vascular graft component separation risk: ADVANTA VXT slider rod defect
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reports of separation between the Slider GDS Swivel Rod and Swivel Core, potentially affecting device functionality.
Product
ADVANTA VXT, 8X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1976-2024·2024-06-12
Vascular graft device recalled for swivel component separation
Atrium Medical recalls ADVANTA VXT vascular grafts due to reports of the Slider GDS Swivel Rod separating from the Swivel Core. The internal component separation could compromise device function.
Product
ADVANTA VXT, 7X50, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1979-2024·2024-06-12
ADVANTA VXT Vascular Graft Slider Component Separation Recall
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the slider rod from its core component. This mechanical failure could compromise device functionality.
Product
ADVANTA VXT, 8X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1291-2024·2024-06-12
Garden Vegetable Cream Cheese Spread recalled for potential Salmonella
Schreiber Foods is recalling Garden Vegetable Cream Cheese Spread sold under multiple brands due to potential Salmonella contamination. Approximately 835,721 units were distributed to 19 states and Puerto Rico.
Product
Garden Vegetable Cream Cheese Spread. Net Wt 8 oz. (226g). Keep Refrigerated, packaged under the following brands: 1. Fareway, UPC 0 21333-83053 9. Packed for Fareway Store, Inc. Boone, Iowa 50036. 2. Essential Everyday, UPC 0 41303-00625 2. Distributed By Supervalu Inc., Eden…
Category
Food
Distribution
20 states