State

Florida product recalls

72,986 recalls have nationwide distribution and so reach Florida. 12,821 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total: 12,821
Critical: 1,765
Severe: 2,975
Most recent: 2026-09-16

Of the 12,821 recalls naming Florida we have scored against our rubric, 1,765 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,975 (23%) are Severe.

Which agencies issued them

These figures cover only the 12,821 recalls whose distribution notice names Florida specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6726–6750 of 85807

SevereFDA (Drugs)·D-0481-2025·2025-07-02
Semaglutide/Cyanocobalamin Injectable Syringes Recalled for Lack of Sterility Assurance
Thrive Health Solutions is recalling Semaglutide/Cyanocobalamin Injectable pre-filled syringes due to lack of assurance of sterility. The affected lot was distributed nationwide.
Product
Semaglutide/Cyanocobalamin Injectable, 5mg/1mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0486-2025·2025-07-02
Tirzepatide/Cyanocobalamin Injectable Recalled Due to Sterility Assurance Failure
Thrive Health Solutions is recalling one lot of Tirzepatide/Cyanocobalamin Injectable pre-filled syringes due to lack of assurance of sterility. The affected product is Lot C03125A distributed nationwide.
Product
Tirzepatide/Cyanocobalamin Injectable, 30mg/1mg/mL (15mg/0.5mg/0.5mL), pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0491-2025·2025-07-02
Sodium Chloride Injection Recalled for Sterility Assurance Defect
B Braun Medical Inc. is recalling 187,656 containers of 0.9% Sodium Chloride Injection USP due to potential sterility failures caused by pinholes in finger boxes during manufacturing. The defect may allow leaks and compromise the sterile nature of the intravenous medication.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0494-2025·2025-07-02
Ketorolac Tromethamine Ophthalmic Solution Recalled for Sterility Risk
Apotex Corp. is recalling Ketorolac Tromethamine Ophthalmic Solution 0.5% due to lack of assurance of sterility. The recall affects 87,840 bottles distributed nationwide.
Product
KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0480-2025·2025-07-02
Semaglutide pre-filled syringe recalled due to sterility concerns
Thrive Health Solutions is recalling Semaglutide 5 mg/mL pre-filled syringes distributed nationwide because the manufacturer cannot assure the product's sterility.
Product
Semaglutide, 5 mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2023-2025·2025-07-02
BD BACTEC MGIT 960 PZA Kit tuberculosis susceptibility testing recall
Becton Dickinson is recalling BD BACTEC MGIT 960 PZA Kit due to reports of intermittent false resistance results during pyrazinamide susceptibility testing of Mycobacterium tuberculosis. The issue affects units distributed worldwide.
Product
BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0473-2025·2025-07-02
Metoclopramide Tablets Recalled for Presence of Foreign Tablets
Teva Pharmaceuticals USA, Inc. is recalling Metoclopramide Tablets, USP 10 mg due to the presence of foreign tablets or capsules in the product. The affected lot is distributed nationwide.
Product
METOCLOPRAMIDE — METOCLOPRAMIDE (METOCLOPRAMIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1904-2025·2025-07-02
Broselow Pediatric Emergency Rainbow Tape recalled for incorrect dosing values
SunMed Holdings is recalling Broselow Pediatric Emergency Rainbow Tape due to incorrect values printed on the tape that could lead to improper medication dosing and defibrillation in pediatric emergency care.
Product
Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev 2 Print Version The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0477-2025·2025-07-02
LX Bioboost Plus Pre-filled Syringe Recalled for Sterility Assurance
Thrive Health Solutions is recalling LX Bioboost Plus pre-filled syringes due to lack of assurance of sterility. The affected product is a multi-ingredient injectable formulation distributed nationwide.
Product
LX Bioboost Plus, (Each 1mL contains Methionine 25 mg, Inositol 50 mg, Choline Chloride 50 mg, Pyridoxine HCl 25 mg, Dexpanthenol 25 mg, Cyanocobalamin 1 mg, L-Arginine HCl 15 mg, L-Carnitine 15 mg, and Lidocaine 1 mg in SWFI), pre-filled syringe, Thrive Health Solutions, 88 Inve
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0478-2025·2025-07-02
NAD+ Pre-Filled Syringes Recalled for Lack of Sterility Assurance
Thrive Health Solutions is recalling NAD+ 100mg/mL pre-filled syringes (Lot #O-O8A01-25) distributed nationwide due to lack of assurance of sterility. Consumers should not use this product.
Product
Nicotinamide adenine dinucleotide (NAD+): 100mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0482-2025·2025-07-02
Tirzepatide Injections Recalled for Lack of Sterility Assurance
Thrive Health Solutions is recalling Tirzepatide Injections (10mg/mL, pre-filled syringes) distributed nationwide due to lack of assurance of sterility. Consumers should not use the affected product and contact their healthcare provider.
Product
Tirzepatide Injections, 10mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0495-2025·2025-07-02
Azelastine Hydrochloride Ophthalmic Solution Recalled Due to Sterility
Apotex Corp. is recalling Azelastine Hydrochloride Ophthalmic Solution, USP 0.05% due to lack of assurance of sterility. The affected batch was distributed nationwide.
Product
AZELASTINE HYDROCHLORIDE — AZELASTINE HYDROCHLORIDE (AZELASTINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0476-2025·2025-07-02
LL Bioboost Injectable pre-filled syringes recalled for lack of sterility assurance
Thrive Health and Wellness, LLC is recalling LL Bioboost Injectable pre-filled syringes nationwide due to lack of assurance of sterility. The affected product is Lot #H277639 with expiration 6/25/2025.
Product
LL Bioboost Injectable, Each 1mL contains Methionine 25 mg, Inositol 50 mg, Choline Chloride 50 mg, and Cyanocobalamin 1 mg in SWFI, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1958-2025·2025-07-02
Extended Tip Applicator 8CM distributed by Integra LifeSciences recalled nationwide
Integra LifeSciences is recalling Extended Tip Applicator 8CM devices due to potentially out-of-specification endotoxin levels and lack of sterility assurance. The recall affects 6,216 units distributed across the US and internationally.
Product
Extended Tip Applicator, 8CM, Box of 5.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1961-2025·2025-07-02
MicroMyst Applicator recalled due to lack of sterility assurance
Integra LifeSciences Corp. is recalling the MicroMyst Applicator Box of 5 due to lack of sterility assurance. The product is used with the Integra Flow Source for controlled application of two liquids.
Product
MicroMyst Applicator, Box of 5. Consisting of a multilumen applicator and filtered line for use with the Integra Flow Source for the controlled application of two liquids.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1960-2025·2025-07-02
Extended Tip Applicator 8CM medical devices recalled due to sterility concerns
Integra LifeSciences is recalling Extended Tip Applicator 8CM devices nationwide and internationally because they may contain potentially out-of-specification endotoxin levels and lack sterility assurance.
Product
Extended Tip Applicator 8CM, Box of 1.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0496-2025·2025-07-02
Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution Recall
Apotex Corp. is recalling 6,288 bottles of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution nationwide due to lack of assurance of sterility. The affected batch (VC6058, expiration date 10/31/2025) does not meet sterility requirements for ophthalmic use.
Product
BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION — BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION (BRIMONIDINE TARTRATE AND TIMOLOL MALEATE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25V447000·2025-07-02
Blue ARC BA4L-800 Recalled for Parking Brake Defect
Shyft Group is recalling 2024-2025 Blue ARC BA4L-800 vehicles because a brake caliper spacer may be too big, preventing the parking brake from engaging properly.
Product
BLUE ARC — BLUE ARC BA4L-800
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1959-2025·2025-07-02
Extended Tip Applicator 15 CM recalled for endotoxin and sterility issues
Integra LifeSciences is recalling Extended Tip Applicators (15 CM, Box of 5) because they may contain out-of-specification levels of endotoxins and lack sterility assurance.
Product
Extended Tip Applicator, 15 CM, Box of 5.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2008-2025·2025-07-02
Altivate Reverse Torx Peripheral Screw labeling mismatch recall
Encore Medical is recalling Altivate Reverse Torx Peripheral Screws because package labeling indicates a different screw size than the product actually included. This mismatch could lead to incorrect surgical implantation.
Product
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number: 506-04-126 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
Category
Medical Device
Distribution
18 states
HighNHTSA·25V409000·2025-07-02
Polestar 2 May Lose Brake Function While Using One Pedal Drive
Certain 2021 and 2024 Polestar 2 vehicles may lose brake function while coasting downhill and using One Pedal Drive mode. Polestar will provide a free over-the-air software update to fix the control module defect.
Product
POLESTAR — POLESTAR POLESTAR 2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2034-2025·2025-07-02
Philips Spectral CT Computed Tomography X-ray System Software
Philips Spectral CT systems with affected software may experience unintended motion of the gantry or table that could lead to contact with operators or patients. Additional software issues may also affect CT performance.
Product
Spectral CT. Computed tomography X-ray system.
Category
Medical Device
Distribution
19 states
HighFDA (Devices)·Z-2028-2025·2025-07-02
REMISOL Advance Medical Device Software Defect Affecting Reference Range Calculations
A software issue in REMISOL Advance may incorrectly process date-of-birth information from laboratory systems, causing incorrect reference range calculations and potentially auto-validating erroneous test result flags. The actual test results are not changed, but their evaluation may be affected.
Product
REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164; C44703; C57017; C69412; C69413; C73942; C73941; C88470; C88471 The Normand Info REMISOL Advance Data Manager collects and manages data and workflow for 128 con
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2018-2025·2025-07-02
CDI OneView System BPM Probe temperature sensor measurement inaccuracy
Terumo Cardiovascular Systems is recalling CDI OneView System BPM Probe units due to thermistor assembly errors that cause inaccurate temperature and blood gas measurements, potentially leading to inappropriate clinical decisions.
Product
CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe, Cat. No. CDI753TK - CDI OneView BPM Probe Trial Kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1997-2025·2025-07-02
Bigfoot Unity Diabetes Management System Pen Caps Unresponsive Due to Firmware Error
Bigfoot Biomedical is recalling Bigfoot Unity Diabetes Management System Pen Caps due to a firmware issue that may cause insulin pens to become unresponsive. People with diabetes may lack information needed to make timely treatment decisions.
Product
Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen Cap LCAP Firmware 1.3.0 Release Configuration, Rev H SW-300689-02 Bigfoot Inject v1 Pen Cap RCAP Firmware 1.3.0 Release Configuration, Rev H The Bigfoot Unity Diabetes Management System that include the
Category
Medical Device
Distribution
Distributed nationwide