The Recall Desk

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.

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.

6626–6650 of 85807

  • SevereFDA (Food)·H-0141-2025·2025-07-09

    Zenshi crunchy dragon tuna brown rice rolls used recalled cucumbers

    Zenshi Handcrafted Sushi Crunchy Dragon Roll with tuna on brown rice is being recalled over cucumbers recalled for possible Salmonella. 398 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Crunchy Dragon Roll - Tuna 10pc (Brown Rice) Net Wt. 9.6oz UPC 0 23012 94462 9
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0175-2025·2025-07-09

    ZENSHI Handcrafted Sushi Hybrid Yon Tray recalled for possible Salmonella

    Harris Teeter is recalling ZENSHI Handcrafted Sushi Hybrid Yon Tray (50pc, 53.8oz) because cucumbers used in the sushi were recalled due to possible Salmonella contamination.

    Product
    ZENSHI HANDCRAFTED SUSHI Hybrid Yon Tray 50pc Net Wt. 53.8oz UPC 0 23012 94261 8
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0120-2025·2025-07-09

    Zenshi arroz picante imitation crab rolls used recalled cucumbers

    Zenshi Handcrafted Sushi Arroz Picante Roll with imitation crab is being recalled over cucumbers recalled for possible Salmonella. 202 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Arroz Picante Roll - Imitation Crab 10pc Net Wt. 10.3oz (292g) UPC 0 23012 94034 8
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0128-2025·2025-07-09

    Zenshi chef sampler A6 sushi trays made with recalled cucumbers

    Zenshi Handcrafted Sushi Chef Sampler A#6 is being recalled over cucumbers recalled for possible Salmonella. 12,774 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Chef Sampler A#6 (Chili, Nigiri, Rainbow) 13pc Net Wt. 13.4oz (380g) UPC 0 23012 94334 9
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0133-2025·2025-07-09

    ZENSHI Handcrafted Sushi Classic Crab Roll Sushi Recalled for Salmonella

    Harris Teeter is recalling ZENSHI Handcrafted Sushi Classic Crab Roll (10.5 oz) because cucumbers used to make the sushi were recalled due to possible Salmonella contamination.

    Product
    ZENSHI HANDCRAFTED SUSHI Classic Crab Roll Sushi Net Wt. 10.5oz UPC 0 23012 00702 7
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2035-2025·2025-07-09

    BiPAP V30 Auto ventilators are not indicated for respiratory failure

    The Philips Respironics BiPAP V30 Auto Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 5,958 units affected.

    Product
    BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2037-2025·2025-07-09

    BiPAP A40 ventilators are not indicated for respiratory failure patients

    The BiPAP A40 Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 6 units in the US and 67,534 outside it are affected.

    Product
    BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients. BiPAP A40 Pro - sold OUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2072-2025·2025-07-09

    Cardiology hemodynamics software update may cause unexpected system shutdowns

    Change Healthcare Cardiology Hemodynamics Software version 15.0.1 is being recalled because, following complaints, a software update may cause the software to unexpectedly shut down.

    Product
    Change Healthcare Cardiology Hemodynamics Software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2089-2025·2025-07-09

    ADVIA Hematology System Control Product Recall for Platelet Value Error

    Siemens Healthcare Diagnostics is recalling 3,266 units of ADVIA 120/2120/2120i 3-in-1 TESTpoint Control worldwide due to incorrect platelet value assignments that could affect test results.

    Product
    ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2058-2025·2025-07-09

    Philips S5-1 Ultrasound Transducers Refurbished Beyond Useful Life

    Philips Ultrasound is recalling Philips S5-1 Transducers because they were refurbished beyond their useful life, which may affect device performance and safety.

    Product
    Philips S5-1 Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2079-2025·2025-07-09

    BD FACS 7-Color Setup Beads Recalled Due to Spectral Overlap Errors

    Becton, Dickinson and Company is recalling BD FACS 7-Color Setup Beads (REF 666289, Lots 85637 and 85638) because errors in the spectral overlap factors table may prevent accurate setup of flow cytometry instruments.

    Product
    REF: 666289 , BD FACS, 7-Color Setup Beads, 25 Runs, CE, IVD. Used in flow cytometry for fluorescence compensation.
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Drugs)·D-0501-2025·2025-07-09

    Compounded ketamine multi-dose vials recalled over sterility assurance concerns

    Ketamine Hydrochloride Injection 500 mg/5 mL multi-dose vials compounded by Medivant Healthcare are being recalled for lack of assurance of sterility. 14,725 vials are affected.

    Product
    KETAmine Hydrochloride Injection, USP, 500mg/5mL, (10mg/mL), For IM or Slow IV Use, 5mL Sterile Multi-Dose Vial, Rx Only, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ 85226, NDC 81483-0007-2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0138-2025·2025-07-09

    Harris Teeter Sushi Rolls Recalled Over Salmonella Risk

    Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Crunchy CA Roll trays because the cucumbers used in the sushi may be contaminated with Salmonella.

    Product
    ZENSHI HANDCRAFTED SUSHI Crunchy CA Roll 10pc Net Wt 8.1oz UPC 0 23012 94283 0 & UPC 0 23012 95144 3
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-2039-2025·2025-07-09

    VITROS XT 7600 Chemistry Analyzer Software Anomaly Causing Erroneous Test Results

    Ortho-Clinical Diagnostics is recalling VITROS XT 7600 Integrated System analyzers due to a software anomaly that can report test results as expired when reagent shelf expiration dates are omitted during manual loading, potentially causing erroneous or delayed test results.

    Product
    Brand Name: VITROS; Product Name: VITROS XT 7600 Integrated System; Model/Catalog Number: (1) 6844461, (2) 6272222; Software Version: version 3.2 to version 3.8.3 (all available software versions); Product Description: In vitro diagnostic chemistry analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2040-2025·2025-07-09

    VITROS 4600 chemistry systems may report results using expired diluent packs

    VITROS 4600 Chemistry Systems are being recalled because a software anomaly can allow results to be reported using diluent packs the system treats as expired, which can produce erroneous results.

    Product
    Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog Number: (1) 6802445, (2) 6900440 Software Version: version 3.2 to version 3.8.3 (all available software versions) Product Description: In vitro diagnostic chemistry analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0203-2025·2025-07-09

    Peak Cocktails blood orange spritz cans may overpressurize and explode

    Peak Cocktails Blood Orange Spritz in 8.4 fl oz cans is being recalled because of overpressurization leading to exploding cans. 16,128 units are affected.

    Product
    Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24, and 48 cans. Batch Codes: B25127, B25128; Packaging Date: 05/07/2025, 05/08/2025
    Category
    Food
    Distribution
    50 states
  • HighFDA (Devices)·Z-2045-2025·2025-07-09

    Medline retinal packs recalled because catheter needle may fail to retract

    Medline RETINAL PACK-LF convenience kits are being recalled because the BD Insyte Autoguard catheter needle inside may be slow to retract or fail to retract during insertion. 80 units affected.

    Product
    Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: RETINAL PACK-LF, REF DYNJ0151148B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0117-2025·2025-07-09

    Three Milk Mousse cups recalled for undeclared allergens

    Sabores Fit Bakery is recalling Three Milk Mousse cups because the label fails to declare allergens including milk, eggs, soy, wheat, and tree nuts. Consumers with allergies to these ingredients should not consume the product.

    Product
    Three Milk Mousse, NET WT 8 OZ (230g), Sabores Bakery, Plastic Cups, 3.5-inch-wide x 3.75 in high, Keep refrigerated, PRODUCED EXCLUSIVELY BY: SABORES FIT BAKERY LLC. ORLANDO, FL 32836, UPC 7 35816 97176 2
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0116-2025·2025-07-09

    Passion Fruit Mousse Recalled for Undeclared Allergens

    Sabores Fit Bakery is recalling Passion Fruit Mousse (8 oz cups) because the label fails to declare milk, eggs, soy, wheat, and tree nuts allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    Passion Fruit Mousse, NET WT 8 OZ (230g), Sabores Bakery, Plastic Cups, 3.5-inch-wide x 3.75 in high, Keep refrigerated, PRODUCED EXCLUSIVELY BY: SABORES FIT BAKERY LLC. ORLANDO, FL 32836, UPC 7 35816 97176 2
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2069-2025·2025-07-09

    Apex Knee System components recalled over loss of sterile packaging integrity

    Apex Knee System components are being recalled because the age of the nylon packaging material has caused a loss of integrity of some pouches. 341 units are affected.

    Product
    Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-50137, KC-50150, KC-50155, KC-50157, KC-50170, KC-50175, KC-50177, KC-50190, KC-50197, KC-52104, KC-52554, KC-52574, KC-52774, KC-55223, KC-55243
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0144-2025·2025-07-09

    Harris Teeter Sushi Rolls Recalled Over Salmonella Risk

    Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Crunchy Roll - Salmon products due to possible Salmonella contamination from recalled cucumbers used in production.

    Product
    ZENSHI HANDCRAFTED SUSHI Crunchy Roll - Salmon 10pc Net Wt. 10.0oz UPC 0 23012 95040 8
    Category
    Food
    Distribution
    8 states
  • HighFDA (Drugs)·D-0500-2025·2025-07-09

    Compounded ketamine injection recalled over lack of sterility assurance concerns

    Ketamine Hydrochloride Injection compounded by Medivant Healthcare is being recalled for lack of assurance of sterility after an FDA inspection raised concerns about the sterile manufacturing process.

    Product
    KETAmine Hydrochloride Injection, USP, 50 mg/5mL (10 mg/mL), For IM Use or Slow IV Use, 5 mL Sterile Single-Dose Vial, Rx Only, For Office Use Only, Compounded Durg by: Medivant Healthcare, 158 S. Kyrene Rd. Chandler, AZ 85226, NDC 81483-0006-0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2051-2025·2025-07-09

    Philips C9-5EC Ultrasound Transducer Devices Recalled

    Philips Ultrasound, Inc. is recalling Philips C9-5EC transducer devices that were refurbished beyond their useful life, which may affect device performance and safety.

    Product
    Philips C9-5EC Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0115-2025·2025-07-09

    Choco Mousse cups recalled for undeclared allergens

    Sabores Fit Bakery is recalling Choco Mousse cups because the label does not fully disclose allergens including milk, eggs, soy, wheat, tree nuts (almonds, hazelnuts).

    Product
    Choco Mousse, NET WT 8 OZ (230g), Sabores Bakery, Plastic Cups, 3.5-inch-wide x 3.75 in high, Keep refrigerated, PRODUCED EXCLUSIVELY BY: SABORES FIT BAKERY LLC. ORLANDO, FL 32836, UPC 7 35816 97176 2
    Category
    Food
    Distribution
    1 state