The Recall Desk

State

Florida product recalls

72,940 recalls have nationwide distribution and so reach Florida. 12,818 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,818
Critical
1,764
Severe
2,975
Most recent
2026-09-09

Of the 12,818 recalls naming Florida we have scored against our rubric, 1,764 (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 12,818 recalls whose distribution notice names Florida specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3626–3650 of 85758

  • CriticalFDA (Devices)·Z-1115-2026·2026-02-04

    Broselow Rainbow Tape 7700RE recalled over potentially harmful dosing errors

    SunMed Holdings is recalling 20,583 units of the Broselow Pediatric Emergency Rainbow Tape, model 7700RE, because it contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.

    Product
    Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700RE Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1114-2026·2026-02-04

    Pediatric emergency tapes recalled over potentially harmful drug dosing errors

    SunMed Holdings is recalling 95,300 units of the Broselow Pediatric Emergency Rainbow Tape because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.

    Product
    Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1117-2026·2026-02-04

    Filled Broselow organizers recalled over potentially harmful dosing errors

    SunMed Holdings is recalling 89 units of the Filled Broselow Organizer, model 7730IALS, because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.

    Product
    Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog Number: 7730IALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Comp
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V064000·2026-02-04

    BMW Recalls 2026 Gran Coupe Models for Rear Light Defects

    BMW is recalling 2026 228i and M235i Gran Coupe vehicles because rear lights may not function properly, increasing crash risk.

    Product
    BMW — BMW 228I XDRIVE GRAN COUPE, 228I GRAN COUPE, M235I XDRIVE GRAN COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1173-2026·2026-02-04

    AlternatiV+ screw-in anchors recalled after reports of device failure

    Aju Pharm is recalling 416 units of the AlternatiV+ Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    AlternatiV+ Screw-In Anchor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1220-2026·2026-02-04

    Ingenia 3.0T systems recalled over elastography stiffness value errors

    Philips North America is recalling 24 units of the Ingenia 3.0T MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    BEAR Implant. Model Number: 1000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1171-2026·2026-02-04

    Push-in suture anchors recalled after reports of breakage and pull out

    Aju Pharm is recalling 200 units of the Genesis Push-In Suture Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    Genesis Push-In Suture Anchor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·26252·2026-02-04

    Combination fuel containers recalled over missing flame mitigation devices

    About 700 Scepter B62 gas and oil combination fuel containers are being recalled because they lack flame mitigation devices and the spout is not child-resistant.

    Product
    Scepter Gas and Oil Combination Fuel Containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1209-2026·2026-02-04

    Ingenia Ambition S systems recalled over elastography stiffness value errors

    Philips North America is recalling 1 unit of the Ingenia Ambition S because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Ingenia Ambition S. Product Code (REF): 782108. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1207-2026·2026-02-04

    Dual thread screw-in anchors recalled after reports of device failure

    Aju Pharm is recalling 400 units of the Genesis Dual Thread Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    Ingenia 3.0T. Product Code (REF): (1) 781342, (2) 781377. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1203-2026·2026-02-04

    Chest drainage units recalled to limit their use to adults

    Cardinal Health is updating the instructions for use on 1,169,726 chest drainage units to clarify that the intended patient population is adults 18 years and older.

    Product
    Chest Drainage Units and Accessories: Product Code Description 1. 8888571562 Cardinal Health Sentinel Seal CDU 2. 8888571513 Cardinal Health Sentinel Seal CDU, Dual Drain 3. 8888571489 Cardinal Health Sentinel Seal CDU, with Easy Change Connector 4. 8888571370 Cardinal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1182-2026·2026-02-04

    Feminine hygiene products recalled over rodent activity in a distribution center

    Gold Star Distribution is recalling feminine hygiene products over potential exposure of rodents and rodent activity in its distribution center.

    Product
    Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS THIN LINERS SCENTED 12CT, ALWAYS ULT.THIN WINGS REG.12/22CT, ALWAYS ULT.THIN OVER NIGHT WINGS 12/16CT, JULIE MAXI NIGHT W.WINGS 36/10CT, STAY FREE REG. 12/10CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1204-2026·2026-02-04

    Evolution Upgrade 1.5T systems recalled over elastography stiffness value errors

    Philips North America is recalling 3 units of the Evolution Upgrade 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1205-2026·2026-02-04

    Evolution Upgrade 3.0T systems recalled over elastography stiffness value errors

    Philips North America is recalling 1 unit of the Evolution Upgrade 3.0T MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1174-2026·2026-02-04

    Roasted pumpkin tamales recalled over potential Listeria monocytogenes contamination

    Prima Vera Nueva is recalling 9,656 packages (4 tamales per package) of Roasted Pumpkin & White Cheddar Tamales over potential contamination with Listeria monocytogenes.

    Product
    Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software Version VB10D-SP02
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1212-2026·2026-02-04

    Ingenia Elition X systems recalled over elastography stiffness value errors

    Philips North America is recalling 31 units of the Ingenia Elition X MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1208-2026·2026-02-04

    Ingenia 3.0T CX systems recalled over elastography stiffness value errors

    Philips North America is recalling 6 units of the Ingenia 3.0T CX MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1172-2026·2026-02-04

    Knotless suture anchors recalled after reports of breakage and pull out

    Aju Pharm is recalling 2,569 AlternatiV+ Max Knotless Anchors after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    AlternatiV+ Max Knotless Anchor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1214-2026·2026-02-04

    MR 7700 upgrades recalled over elastography stiffness value errors

    Philips North America is recalling 6 units of the Upgrade to MR 7700 because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Upgrade to MR 7700. Product Code (REF): 782130. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1181-2026·2026-02-04

    Condoms recalled over rodent activity in a distribution center

    Gold Star Distribution is recalling condoms over potential exposure of rodents and rodent activity in its distribution center.

    Product
    Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1168-2026·2026-02-04

    Screw-in suture anchors recalled after reports of breakage and bending

    Aju Pharm is recalling 600 units of the Genesis Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    Genesis Screw-In Anchor
    Category
    Medical Device
    Distribution
    Distributed nationwide