State

Florida product recalls

73,381 recalls have nationwide distribution and so reach Florida. 12,858 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total: 12,858
Critical: 1,775
Severe: 3,453
Most recent: 2026-10-07

Of the 12,858 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 3,453 (27%) are Severe.

Which agencies issued them

These figures cover only the 12,858 recalls whose distribution notice names Florida specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19651–19675 of 86239

HighFDA (Food)·F-0346-2023·2023-02-08
Organic jackfruit recalled for undeclared sulfites in Florida
Organic jackfruit produced by Food Castle, Inc. is being recalled due to undeclared sulfites not listed on the product label. Sulfite-sensitive consumers face potential allergic reaction risk.
Product
ORGANIC JACKFRUIT Nutty and Fruity Brand UNSWEETENED AND UNSULFURED NET WT. 3.5 oz. (100g) USDA ORGANIC UPC: 819496021426 8 units per case Distributed by: Food Castle Inc. Vernon, CA 90058 PRODUCT OF SRI LANKA
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-1045-2023·2023-02-08
MEDLINE UNITE Foot and Ankle Screw Recall: Intra-Operative Failure
MEDLINE INDUSTRIES is recalling 420 units of UNITE Foot and Ankle surgical screws (Lot 810304) due to observed intra-operative failure when pre-drilled and implanted with excessive torque.
Product
MEDLINE UNITE FOOT & ANKLE Screw, Non-Locking, Mini T8 (2.0x8mm), REF MMSN2008
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1023-2023·2023-02-08
Medtronic Affinity Fusion Oxygenator: Temperature Monitoring Adapter May Detach
Medtronic is recalling 2,937 Affinity Fusion Oxygenators used in cardiac surgery because the Temperature Monitoring Adapter may detach during setup or disassembly.
Product
Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs, REF BB811. Used in Cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1039-2023·2023-02-08
Non-Invasive Patient Tracker Verification Failure During Image-Guided Surgery
Medtronic is recalling AxiEM Non-Invasive Patient Trackers due to increasing complaints that users cannot verify their navigation instruments work properly during image-guided surgery. The verification failure affects approximately 1,867 devices worldwide.
Product
AxiEM" Non-Invasive Patient Tracker
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-1037-2023·2023-02-08
Turbett Surgical Container TS1200 Recalled Due to Potential Weld Failures
Turbett Surgical Container TS1200 units may have weld failures that could breach the sterile barrier, potentially allowing unsterile instruments to be used in medical procedures and risking infection.
Product
Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1028-2023·2023-02-08
Medtronic Perfusion Oxygenator Temperature Monitoring Adapter Detachment Recall
Medtronic has recalled Custom Pack Perfusion Tubing Packs used in cardiopulmonary bypass procedures. The Temperature Monitoring Adapter on the oxygenator may detach during setup or disassembly.
Product
Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, REF CB811. Used in Cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1042-2023·2023-02-08
Vanguard Knee System Prosthesis Components Incorrectly Labeled for Size and Side
Biomet is recalling 157 units of Vanguard Knee System prosthesis components incorrectly labeled as different sizes or surgical sides. Surgeons relying on labels could implant the wrong size or side, requiring corrective surgery.
Product
(1) Vanguard Knee System PS Open Box Femoral; Right; 60 mm. Intended for knee joint replacement prostheses. Item Number: 183104 (2) Vanguard Knee System PS Open Box Femoral; Right; 62.5 mm Item Number: 183106 (3) Vanguard Knee System PS Open Box Femoral; Right; 65 mm Item…
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-1032-2023·2023-02-08
Non-sterile procedural trays with potential sterile packaging breach
Medline Industries is recalling non-sterile procedural trays containing sterile blades that may damage sterile packaging due to blade puncture risk. Lot 22IBQ980. No illnesses reported.
Product
Non-sterile procedural trays labeled as MAJOR/MINOR, 3 per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1048-2023·2023-02-08
GORE CARDIOFORM Septal Occluder Recalled for Incomplete Quality Documentation
W L Gore & Associates is recalling 14 units of the GORE CARDIOFORM Septal Occluder (GSX0030A) due to incomplete quality test documentation. The missing verification of device release could pose a potential risk of device failure and serious complications.
Product
GORE CARDIOFORM Septal Occluder, REF: GSX0030A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0262-2023·2023-02-08
Diltiazem Hydrochloride extended-release capsules recalled due to failed quality specifications
Sun Pharmaceutical is recalling Diltiazem Hydrochloride Extended-Release Capsules (360 mg) due to failed impurity specifications and dissolution testing found during FDA laboratory evaluation. The recall affects five lot numbers distributed nationwide.
Product
DILTIAZEM HYDROCHLORIDE — DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1022-2023·2023-02-08
SynCardia Total Artificial Heart System Recalled for Cannula Tears
SynCardia Systems is recalling its Total Artificial Heart System due to reported tears in the cannula caused by wear and tear stress. Approximately 1,732 systems worldwide are affected.
Product
SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1038-2023·2023-02-08
Turbett Surgical Container TS1000 may have weld failures breaching sterile barrier
Turbett Surgical Container TS1000 may have weld failures that breach the sterile barrier, potentially resulting in unsterile instruments being used in medical procedures and risking patient infection or injury.
Product
Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1047-2023·2023-02-08
Medline UNITE Foot & Ankle Drill Bit Recalled for Intra-operative Screw Failure Risk
Medline Industries recalls 190 UNITE foot and ankle drill bits due to observed screw failure during surgery. When used to pre-drill holes for certain screw sizes, the drill bits may fail under surgical torque, creating risk during procedures.
Product
MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1030-2023·2023-02-08
Non-sterile procedural trays risk sterile packaging breach
Medline Industries is recalling non-sterile laparoscopic procedural trays containing sterile blades that may puncture the outer packaging, potentially breaching the sterile barrier. 260 cases have been distributed nationwide.
Product
Non-sterile procedural trays labeled as LAPAROSCOPIC, 2 per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1029-2023·2023-02-08
MEDLINE procedural trays recalled for potential sterile packaging breach
MEDLINE is recalling procedural trays because sterile blades within the kits could puncture the outer foil packaging, potentially breaching the sterile barrier.
Product
Non-sterile procedural trays labeled as CRANI, 2 per case
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·23115·2023-02-08
Fabuloso Multi-Purpose Cleaners Recalled for Bacterial Contamination Risk
Colgate-Palmolive is recalling about 4.9 million Fabuloso Multi-Purpose Cleaners due to contamination with Pseudomonas bacteria. People with weakened immune systems, external medical devices, or underlying lung conditions face a risk of serious infection from exposure.
Product
Fabuloso Multi-Purpose Cleaners
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1027-2023·2023-02-08
Temperature Monitoring Adapter Detachment in Cardiopulmonary Bypass Oxygenators
Medtronic is recalling cardiopulmonary bypass equipment because the Temperature Monitoring Adapter can come loose during setup or disassembly, potentially compromising temperature monitoring during heart surgery.
Product
Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, REF BB811. Used in Cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1043-2023·2023-02-08
Biomet Vanguard Knee Implant Components Recalled for Incorrect Labeling
Biomet, Inc. is recalling specific Vanguard Knee System prosthetic components that are incorrectly labeled with wrong sizes and sides. This labeling error could result in incorrect implant placement during knee replacement surgery.
Product
(1) Vanguard Knee System PS Open Box Femoral; Left; 57.5 mm. Intended for Knee joint replacement prostheses. Item Number: 183122 EXPANDED RECALL: (2) Vanguard Knee System PS Open Box Femoral; Left; 60 mm. Item Number: 183124 (3) Vanguard Knee System PS Open Box Femoral…
Category
Medical Device
Distribution
6 states
ModerateFDA (Food)·F-0323-2023·2023-02-08
Vitamin B Complex dietary supplement recalled due to undeclared niacin
Professional Complementary Health Formulas, LLC recalls Vitamin B Complex dietary supplement (lot 1092715) due to undeclared niacin affecting 299 bottles distributed nationwide.
Product
Vitamin B Complex packaged in white plastic bottle labeled in part, "***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Vitamin B Complex DIETARY SUPPLEMENT 60 Capsules***Supplement Facts Serving Size: One Capsule***Vitamin B1 (as thiamine Hcl) 80mg 6667% Vitamin B2 (as riboflavin)…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0322-2023·2023-02-08
Inositol dietary supplement recalled due to undeclared niacin
Professional Complementary Health Formulas is recalling Inositol dietary supplement (Lot 1032526, UPC 4065111562) distributed in NY, OR, PA, UT, WI, and WY due to undeclared niacin. Consumers should stop using the product.
Product
Inositol packaged in white plastic bottle with UPC 4065111562 and labeled in part, "***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Inositol DIETARY SUPPLEMENT 360 Capsules***Supplement Facts Serving Size: One Capsule***Inositol 920 mg***Other Ingredients: Vegetarian capsule…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1049-2023·2023-02-08
Lucid TCD 2.0 Transcranial Ultrasound System Recalled for Hard Drive Failure
The Lucid TCD 2.0 System has a faulty hard drive that causes the device to freeze and reboot. Eventually, the system becomes completely inoperable.
Product
Lucid TCD 2.0 System, Model: NA-LUCM1. Transcranial Ultrasound System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0261-2023·2023-02-08
Homeopathic Topical Cream Recalled for Manufacturing Process Deviations
DISCOVERY PHARMA LLC voluntarily recalled 21,892 tubes of Conzerol zero molluscum contagiosum topical cream distributed in California, Florida, and Washington due to current good manufacturing practice deviations.
Product
Conzerol zero molluscum contagiosum, Homeopathic treatment for Molluscum Contagiosum, Topical Cream, Net weight 0.78 oz (22g) tube, UPC 8 60322 00180 8, Manufactured by: Dr. Retter EC Warszawska 17, 05-075 Warszawa Poland
Category
Drug
Distribution
3 states
ModerateFDA (Devices)·Z-1050-2023·2023-02-08
Ultrasound system hard drive defect causes device freezing and failure
FDA recall of NovaGuide Intelligent Ultrasound System due to faulty hard drive causing device freezing and eventual system failure.
Product
NovaGuide Intelligent Ultrasound System, Model: NA-RBTSYS1. Comprised of NovaBot Automated Headset (AKA: NeuralBot, Model: NA-RBT1) and Lucid TCD 2.0 Transcranial Doppler Ultrasound (Model: NA-LUCM1)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1041-2023·2023-02-08
Biopsy marker device recalled for label and contents mismatch
Carbon Medical Technologies recalls 550 Mammotome MammoStar biopsy markers due to a labeling error. The label identifies one product but the package contains a different marker size and shape.
Product
Mammotome MammoStar Biopsy Site Identified, REF STAR1401
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V055000·2023-02-07
Newell Recalls 2023 P50 Motor Coaches Due to Battery Disconnect Switch Defect
Newell Coach Corp. is recalling 2023 P50 motor coaches because the battery disconnect switch may fail to turn off, increasing the risk of electrical shock during maintenance.
Product
NEWELL — NEWELL P50
Category
Vehicle
Distribution
Distributed nationwide