The Recall Desk

State

Florida product recalls

72,820 recalls have nationwide distribution and so reach Florida. 12,816 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,816
Critical
1,763
Severe
2,974
Most recent
2026-09-06

Of the 12,816 recalls naming Florida we have scored against our rubric, 1,763 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,974 (23%) are Severe.

These figures cover only the 12,816 recalls whose distribution notice names Florida specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

101–125 of 85636

  • ModerateFDA (Devices)·Z-3000-2026·2026-09-02

    American Contract System Convenience Kit Recalled for Performance Failures

    American Contract Systems Inc is recalling 30 units of Convenience Kits containing Medline catheters because samples failed performance specifications.

    Product
    American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3001-2026·2026-09-02

    American Contract Systems Recalls Convenience Kits with Non-Conforming Catheters

    American Contract Systems Inc is recalling 30 units of Convenience Kits because the included Medline catheters did not meet performance specifications.

    Product
    American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3016-2026·2026-09-02

    Henry Schein Recalls Dental Composite Capsules Due to Incorrect Packaging

    Henry Schein Inc. is recalling specific lots of Grandio Universal Nano-Hybrid Restorative Material capsules because they were distributed with incorrect packaging and Instructions for Use.

    Product
    Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm, Product Codes: 1) 949-3594, Mfr Product Code 1840; Lots 2529604, 2538147, 2608145 2) 949-3595, Mfr Product Code 1841; Lots 2539075, 2539313, 2609789, 2539065 3) 949-3596, Mfr Product Code 1842; Lots 253663
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3003-2026·2026-09-02

    American Contract System Convenience Kit Recalled for Performance Failures

    American Contract Systems Inc is recalling 12 Convenience Kits containing Medline catheters because samples failed performance specifications.

    Product
    American Contract System Convenience Kit, D & C PACK, Model/Catalog Number: LLPD90H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3010-2026·2026-09-02

    AVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency

    AVID Medical, Inc. is recalling 130 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.

    Product
    Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3006-2026·2026-09-02

    AVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency

    AVID Medical is recalling 63 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.

    Product
    Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3008-2026·2026-09-02

    AVID Medical Recalls Halyard Total Joint Kits Due to Latex Labeling Error

    AVID Medical is recalling 78 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.

    Product
    Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3030-2026·2026-09-02

    Fujifilm Synapse PACS Software Recalled for Inaccurate Ruler Measurements

    Fujifilm is recalling Synapse PACS software v7.4.310 because a software issue may cause ruler measurements to be inaccurate.

    Product
    FUJIFILM Synapse PACS software v7.4.310; radiological image processing system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0804-2026·2026-09-02

    Apotex Recalls Paxil Tablets for Failed Dissolution and Stability Testing

    Apotex Corp. is recalling 6,972 bottles of Paxil CR 37.5mg tablets because the product failed dissolution specifications and 24-month stability testing.

    Product
    PAXIL — PAXIL (PAROXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2999-2026·2026-09-02

    Medline Trach Tube Kit Recalled for Component Labeling Discrepancy

    Medline is recalling 45 Trach Tube Kits (SKU DYKM2330) due to a component labeling discrepancy. The recall covers units distributed in California.

    Product
    Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3007-2026·2026-09-02

    AVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Error

    AVID Medical, Inc. is recalling 78 Halyard Total Joint kits because the labeling fails to identify that the statlock component contains natural rubber latex.

    Product
    Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3035-2026·2026-09-02

    Olympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling

    Olympus is recalling 335 PowerSeal 5 mm Sealer & Divider devices because the outer shelf box is incorrectly labeled as a 37-cm device.

    Product
    POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V567000·2026-09-01

    Peterbilt Recalls 2027 548 Trucks Due to Brake Valve Size Issues

    PACCAR is recalling 2027 Peterbilt 548 trucks because incorrect front brake valve and hose sizes may delay brake response, increasing crash risk.

    Product
    PETERBILT — PETERBILT 548
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V562000·2026-09-01

    2021-2023 Jeep Grand Cherokee Recall for Rear Coil Spring Defect

    Chrysler is recalling 328,381 Jeep Grand Cherokee vehicles because rear coil springs may detach while driving, increasing crash risk.

    Product
    JEEP — JEEP GRAND CHEROKEE 4XE, GRAND CHEROKEE L, GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V566000·2026-09-01

    Storyteller Overland Recalls MODE and GXV HILT Vans for Fire Risk

    Storyteller Overland is recalling 2026-2027 MODE and 2026 GXV HILT vans because a rooftop fan component may overheat, increasing the risk of a fire.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND GXV HILT, MODE VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V564000·2026-09-01

    Light Boy Recalls GBX12SK Light Towers Due to Frame Bending Risk

    Light Boy is recalling 2020 and 2023 GBX12SK light towers because the trailer frame may bend, causing the tower to detach and become a road hazard.

    Product
    Light Boy — Light Boy GBX12SK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V565000·2026-09-01

    Forest River Transit Buses Recalled for Wheelchair Lift Control Failure

    Forest River is recalling certain 2024-2025 transit buses because a faulty electrical contactor may prevent wheelchair lifts from stopping, increasing injury risk.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS, MOBILITY TRANS STARCRAFT ALLSTAR, GLAVAL UNIVERSAL, SAFETBUS, SENATOR II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V563000·2026-09-01

    Forest River Recalls 2027 Vibe Trailers Due to Carbon Monoxide Risk

    Forest River is recalling 2027 Vibe recreational trailers because the furnace exhaust may not be correctly attached, allowing carbon monoxide to build up inside the cabin.

    Product
    FOREST RIVER — FOREST RIVER VIBE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V559000·2026-09-01

    Jeep Recalls Vehicles Due to Tire Pressure Monitoring System Software Error

    FCA US is recalling specific 2024-2026 Jeep models because a software error may prevent the tire pressure monitoring system from detecting low pressure or illuminating the warning light.

    Product
    JEEP — 2026 JEEP GRAND CHEROKEE 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V557000·2026-08-31

    Tiffin Recalls 2026-2027 Wayfarer RVs Due to LP Tank Defects

    Tiffin is recalling 2026-2027 Wayfarer recreational vehicles because the liquid propane tank may lack a remote shut-off or be loose, posing fire and crash risks.

    Product
    TIFFIN — 2026 TIFFIN WAYFARER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V556000·2026-08-31

    Blue Bird Recalls Vision School Buses Due to Wheelchair Lift Defect

    Blue Bird is recalling 2025-2027 Vision school buses because a faulty electrical contactor may prevent wheelchair lifts from stopping, increasing injury risk.

    Product
    BLUE BIRD — 2025 BLUE BIRD VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V555000·2026-08-31

    Jayco Recalls 2027 Entegra Qwest and Melbourne Prestige RVs

    Jayco is recalling certain 2027 Entegra Qwest and Jayco Melbourne Prestige recreational vehicles due to a taillight harness defect that may cause incorrect warning lights on the instrument panel.

    Product
    JAYCO — JAYCO, ENTEGRA MELBOURNE PRESTIGE, QWEST
    Category
    Vehicle
    Distribution
    Distributed nationwide