The Recall Desk

State

Florida product recalls

20,305 recalls have nationwide distribution and so reach Florida. 0 additional recalls listed Florida specifically in their distribution scope.

About recalls in Florida

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Florida consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

10676–10700 of 20305

  • HighFDA (Drugs)·D-0252-2024·2024-01-24

    Old Spice Anti-Perspirant Spray Recalled Due to Potential Benzene Contamination

    Procter & Gamble is recalling Old Spice SWEAT DEFENSE ULTIMATE CAPTAIN anti-perspirant spray due to potential benzene contamination at the manufacturing facility. Affected products have expiration dates through September 2023.

    Product
    Old Spice, SWEAT DEFENSE ULTIMATE CAPTAIN, Aluminum Chlorohydrate 23.5%, Anti-Perspirant, Topical spray can 3.8 OZ (107 g), Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-385-10, UPC 0 37000 74947 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0764-2024·2024-01-24

    Maquet Axcel Operating Room Light Systems Recalled for Fall Hazard

    The FDA is recalling Maquet Axcel and Axcel+ operating room light systems due to a potential for the light system to fall. The recall affects 236,793 units distributed nationwide and globally.

    Product
    Maquet Axcel / Axcel + OR Light Systems, Model Numbers and Catalog Numbers AXL 5001 - ARD567501961C, AXL 5001S - ARD567505961C, AXL 5002 - ARD567501962C, AXL 5002S - ARD567505962C, AXL 5501 - ARD567501960A, AXL 5501 - ARD567501960C, AXL 5501S - ARD567505960C, AXL+5001 DF - ARD567
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0765-2024·2024-01-24

    Maquet Hanaulux HLX3000 Operating Room Light Systems Recall for Fall Hazard

    Getinge Usa Sales Inc is recalling approximately 236,793 Maquet Hanaulux HLX3000 operating room light systems nationwide and globally due to a potential for the light system to fall in the operating room.

    Product
    Maquet Hanaulux HLX3000 OR Light Systems, Model Numbers and Catalog Numbers H3 BC - HM567811111C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0725-2024·2024-01-24

    Philips Spectral CT 7500 Recalled for Multiple Software Issues Affecting Functionality

    Philips is recalling 197 Spectral CT 7500 computed tomography systems due to multiple software issues affecting device functionality. The devices were distributed nationwide and internationally.

    Product
    Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0245-2024·2024-01-24

    Secret Dry Spray Antiperspirant recalled due to potential benzene contamination

    Procter & Gamble is recalling Secret Dry Spray Antiperspirant due to potential benzene contamination from manufacturing facility issues. No illnesses have been reported.

    Product
    Secret, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Light Essentials, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-382-10, UPC 0 37000 72992 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0229-2024·2024-01-24

    CVS Magnesium Citrate Oral Solution Recalled for Bacterial Contamination

    CVS Health Magnesium Citrate Saline Laxative Oral Solution in Grape flavor is being recalled due to microbial contamination with Acetobacter nitrogenifigens bacteria. Affected lot A80763 (expiration 11/2025) was distributed nationwide.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (CVS MAGNESIUM CITRATE ORAL SOLUTION - GRAPE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0253-2024·2024-01-24

    Secret anti-perspirant spray recalled for potential benzene contamination

    The FDA is recalling Secret powder fresh anti-perspirant spray due to potential benzene contamination found at the manufacturing facility.

    Product
    Secret, powder fresh, (Aluminum chlorohydrate 24%), Anti-Perspirant/Deodorant, Topical spray can Net Wt., (a) 4OZ (113g), NDC 37000-134-11, UPC 0 37000 71109 4, (b) 6OZ (170g), NDC 37000-134-17, UPC 0 37000 71108 7; (c) twin pack-2 Topical spray cans, each can Net Wt. 6OZ (170g)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0747-2024·2024-01-24

    Smiths Medical Injection Line Rotating Adapters Recalled for Seal Defect

    Smiths Medical is recalling specific injection line rotating adapters due to a manufacturing defect causing oversized O-rings that may lead to inadequate seal integrity and medication under-infusion.

    Product
    48IN (121.9CM) INJ LINE ROTATING ADAPT (900psi), List Number MX694R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0750-2024·2024-01-24

    GammaPod Radiation Treatment Planning System Software Error Allows Wrong Imaging Structures

    Xcision Medical Systems recalled 4 GammaPod Treatment Planning Systems due to a software error that allows incorrect radiation structures from previous CT scans to be imported and selected, potentially affecting treatment planning accuracy.

    Product
    GammaPod - Treatment Planning System-a component of the GammaPod Irradiation System. Ref: XMSGP030A09.07-0.01 Intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0741-2024·2024-01-24

    FDA Recalls Medical Pressure Tubing With Defective O-Ring Seals

    Smiths Medical is recalling 31,685 units of pressure tubing with defective O-rings that may not seal properly during medication infusion, potentially causing medication leaks and underdosing. The defect affects specific lot numbers with worldwide distribution.

    Product
    6IN PRESSURE TUBING, List Number MX20617
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0751-2024·2024-01-24

    Medical Device Calibration Serums Recalled Due to Instructional Transcription Errors

    Randox Laboratories has recalled multiple calibration serum products due to transcription errors in the Instructions for Use, which contain incorrect target values for several analytes.

    Product
    Calibration Serum Level 3. CAL 3, REF CAL2351. Human Assayed Multi-Sera Level 2 (HN1530) Human Assayed Multi-Sera Level 3 (HE 1532)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0239-2024·2024-01-24

    Old Spice Anti-Perspirant Spray Recalled Due to Facility Benzene Contamination

    Old Spice SWEAT DEFENSE Dry Spray anti-perspirant is being recalled due to manufacturing facility issues where other product lots were found contaminated with benzene. No illnesses have been reported.

    Product
    Old Spice, SWEAT DEFENSE, STRONGER SWAGGER, Dry Spray, 48 Hour, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical Spray Can, Net WT 3.8 oz (107 g), Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC 69423-386-10, UPC 0 37000 73034 7 OR UPC 0 12044 04475 9 (12 Pack, ol
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0247-2024·2024-01-24

    Secret OUTLAST Dry Spray Antiperspirant recalled for potential benzene contamination

    Procter & Gamble is recalling Secret OUTLAST Dry Spray Antiperspirant due to a manufacturing facility deviation where other lots were found contaminated with benzene. The recalled product was manufactured at the affected facility.

    Product
    Secret, OUTLAST, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Completely Clean, Topical spray can 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-384-10, UPC 0 37000 74764 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0733-2024·2024-01-24

    VACUETTE Blood Collection Tubes Missing Critical Anticoagulant Additive

    VACUETTE blood collection tubes are missing an anticoagulant additive, causing samples to clot and producing inaccurate or absent lab results. This can delay diagnosis or lead to inappropriate treatment.

    Product
    VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate, Item #454297, 13x75 grey cap-black ring, non-ridged.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0746-2024·2024-01-24

    Medex Injection Line Rotating Adapter Recalled Due to O-Ring Defect

    Smiths Medical is recalling Medex injection line rotating adapters due to a manufacturing defect where the O-ring inner diameter may be oversized, potentially causing medication leaks during infusion.

    Product
    Medex 20IN (50.8CM) INJ LINE ROTATING ADAPT, List Number MX682R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0251-2024·2024-01-24

    Old Spice Anti-Perspirant Spray Recalled for Potential Benzene Contamination

    The FDA has recalled Old Spice SWEAT DEFENSE PURE SPORT PLUS anti-perspirant spray due to potential benzene contamination found at the manufacturing facility. All lots through September 2023 are affected.

    Product
    Old Spice, SWEAT DEFENSE PURE SPORT PLUS, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical spray can, Net WT 3.8 oz (107 g) cans, Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-387-10, UPC 0 37000 72974 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0730-2024·2024-01-24

    Ultrasound Examination Table Recalled for Backrest Stress Fracture

    Oakworks Inc is recalling 28 Ultrasound EA examination tables due to backrest platform stress fractures that prevent operation in an inclined position.

    Product
    Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0736-2024·2024-01-24

    BD PosiFlush Prefilled Saline Syringes Recalled for Incorrect Stopper

    Becton Dickinson is recalling 5,085,120 BD PosiFlush Prefilled Saline Syringes due to an incorrect stopper that increases injection force and may trigger pump alarms.

    Product
    PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0230-2024·2024-01-24

    Freskaro Magnesium Citrate oral solution recalled for bacterial contamination

    Pharma Nobis LLC is recalling Freskaro Magnesium Citrate Oral Solution (Grape Flavor) nationwide due to the presence of Acetobacter nitrogenifigens bacteria.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - GRAPE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0737-2024·2024-01-24

    V. Mueller Bandage Scissors recalled for pink dye staining on handles

    Steris Corporation is recalling V. Mueller Universal Bandage Scissors (Model SU2014-001) due to an incorrect resin carrier in the handle cover. Pink dye residue may appear on scissors and sterilization pouches after processing.

    Product
    V. Mueller Universal Bandage Scissors Black Plastic Handles Heavy-Duty, Autoclavable, Overall Length 7 (18 cm)- Intended to cut through tape and bandages Model: SU2014-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·24084·2024-01-18

    Home Design Upholstered Low Profile Beds Recalled for Fall Injury Risk

    Home Design is recalling about 527,177 upholstered low-profile beds sold through Wayfair, Walmart.com, and Overstock.com from July 2018 through November 2023. The beds can break, sag, or collapse during use, creating a fall and injury hazard.

    Product
    Upholstered Low Profile Standard and Platform Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24086·2024-01-18

    Steamist Wall-Mounted Tilt-Up Bath Shower Seats Recalled for Fall and Laceration Hazards

    Steamist is recalling about 3,900 wall-mounted, folding teak wood shower seats because the support rods and mounting brackets can corrode and break, creating fall and laceration hazards. The firm has received 62 reports of the seats breaking, including 4 injury reports.

    Product
    Tilt-Up Bath & Shower Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24085·2024-01-18

    Bokser Home 100% Cotton Mattress Pads Recalled for Fire Hazard

    Bokser Home is recalling about 2,300 units of 100% cotton mattress pads because they violate federal flammability regulations and pose a fire hazard. No injuries have been reported.

    Product
    Bokser Home 100% Cotton Mattress Pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0220-2024·2024-01-17

    Prescription Vigabatrin Powder Recalled for Defective Container Leakage Risk

    InvaGen Pharmaceuticals recalls Vigabatrin for Oral Solution nationwide due to defective containers that may leak. Consumers with affected lot should contact their pharmacy or healthcare provider.

    Product
    VIGABATRIN — VIGABATRIN (VIGABATRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0219-2024·2024-01-17

    Prescription Tacrolimus Capsules Recalled for Wrong-Strength Product Mix

    Dr. Reddy's Laboratories is recalling 8,280 bottles of Tacrolimus 1 mg capsules after a 0.5 mg capsule was found in a bottle. The wrong-strength capsule could cause dosage confusion.

    Product
    TACROLIMUS — TACROLIMUS (TACROLIMUS)
    Category
    Drug
    Distribution
    Distributed nationwide