The Recall Desk

State

Florida product recalls

73,509 recalls have nationwide distribution and so reach Florida. 12,862 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,862
Critical
1,775
Severe
3,455
Most recent
2026-10-14

Of the 12,862 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 3,455 (27%) are Severe.

Which agencies issued them

These figures cover only the 12,862 recalls whose distribution notice names Florida specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24551–24575 of 86371

  • HighFDA (Devices)·Z-0728-2022·2022-03-16

    Stryker Camera Control Unit Recalled Due to Inverted Image Display Defect

    Stryker is recalling the 1688 Camera Control Unit due to a software defect that causes the surgical monitor image to flip upside-down. This could lead to surgeon error or the need for additional surgical intervention.

    Product
    1688 Camera Control Unit (CCU), Catalog number:1688010000. Used in general laparoscopy, nasopharyngoscopy, ear endoscopy, sinuscopy, and plastic surgery wherever a laparoscope/endoscope/arthroscope/sinuscope is used.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0746-2022·2022-03-16

    PCA 4000 Dental Curing Units May Not Fully Cure Resins

    Envisiontec is recalling 172 PCA 4000 curing units that may not properly cure dental resins to specification (SKU ACC-06-1000).

    Product
    PCA 4000 Curing Units, SKU number ACC-06-1000 The PCA 4000 is used for curing industrial resins as well and this recall will not impact units sold to industrial customers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22100·2022-03-16

    Specialized Bicycle Crank Arm Disengagement Recall Poses Fall Hazard

    Specialized is recalling about 19,000 Sirrus bicycles with defective alloy cranks that can disengage and cause falls. The manufacturer has received 30 reports of the defect, but no injuries have been reported.

    Product
    Sirrus, Sirrus X and Sirrus Sport Bicycles with alloy cranks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22102·2022-03-16

    RH Illuminated Mirrors Recalled Due to Fire and Shock Hazards

    RH is recalling about 3,300 illuminated mirrors sold from September 2015 through February 2022 due to loose components in bulb sockets that can cause overcurrent, overheating, fire, and electrical shock. Consumers should stop using them immediately and contact RH for a refund or replacement.

    Product
    Illuminated Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V160000·2022-03-16

    Harley-Davidson Motorcycles Recalled for Detaching Brake Fluid Warning Labels

    Harley-Davidson is recalling certain 2021-2022 XL Sportster motorcycles because brake fluid warning labels may detach from reservoir caps. Missing labels could lead to improper brake maintenance and increased crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON XL883N, XL1200X, XL1200NS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0649-2022·2022-03-16

    Paliperidone Extended-Release Tablets Recalled for Failed Dissolution

    The Harvard Drug Group is recalling 174 cartons of Paliperidone Extended-Release Tablets, 9 mg, nationwide due to failed dissolution specifications. The affected lots are N00522 (Exp. 09/2022) and N00618 (Exp. 11/2022).

    Product
    PALIPERIDONE — PALIPERIDONE (PALIPERIDONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0651-2022·2022-03-16

    Alprazolam 2 mg tablets recalled due to potential cross-contamination

    Direct Rx is recalling Alprazolam C-IV 2 mg tablets (Lot #07NO1901, expiration 5/31/22) distributed in Florida, Georgia, and Louisiana due to potential cross-contamination identified at the contract manufacturer Ultra Tab Laboratories Inc.

    Product
    Alprazolam C-IV 2 mg, 60-count bottles, Rx Only, Dist. By: Par Pharmaceutical Chestnut Ridge, NY 10977 Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, NDC 72189-0058-60
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0650-2022·2022-03-16

    Alprazolam 1 mg recalled for potential cross-contamination at manufacturer

    Direct Rx is recalling Alprazolam C-IV 1 mg 60-count bottles due to potential cross-contamination at the contract manufacturer, Ultra Tab Laboratories Inc. The recall affects 16 bottles distributed to Florida, Georgia, and Louisiana.

    Product
    Alprazolam C-IV 1 mg 60-count bottles, Rx Only, Dist. By: Par Pharmaceutical Chestnut Ridge, NY 10977 Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, NDC 61919-836-60
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0731-2022·2022-03-16

    Celltrion DiaTrust COVID-19 Rapid Test Kits Recalled for Incorrect Expiration Dates

    Celltrion USA Inc. is recalling 1.2 million DiaTrust COVID-19 rapid test kits due to incorrect expiration dates on packaging. The kits were distributed to 11 states.

    Product
    Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0723-2022·2022-03-16

    CIRRUS HD-OCT Optic Nerve Angiography Feature Requires Deactivation

    Carl Zeiss Meditec is recalling CIRRUS HD-OCT Models 5000 and 6000 AngioPlex devices. The optic nerve head angiography feature was distributed without FDA pre-market clearance and must be disabled.

    Product
    CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0744-2022·2022-03-16

    PuraSinus Nasal Hemostat Recalled Due to Unvalidated Shipping Boxes

    3-D Matrix, Inc. is recalling PuraSinus Absorbable Nasal Hemostat units because the shipping boxes used for transport were not validated.

    Product
    PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V158000·2022-03-15

    Kia Recalls 2014-2016 Cadenza for Windshield Bonding Defect

    Kia is recalling 2014-2016 Cadenza vehicles because the front windshield may not be properly bonded, posing a risk of detachment.

    Product
    KIA — KIA CADENZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V159000·2022-03-15

    Great Dane Recalls 2022 Trailers Due to Loose Suspension Bolts

    Great Dane is recalling 2022 Champion and Everest trailers because suspension bolts were not properly tightened, posing a crash risk.

    Product
    GREAT DANE — GREAT DANE CHAMPION, EVEREST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V157000·2022-03-15

    2022 Winnebago travel trailers recalled for improperly welded couplers

    Winnebago is recalling certain 2022 Micro Minnie, Minnie, and Voyage travel trailers because the coupler was improperly welded, which may cause the trailer to separate from the tow vehicle and increase crash risk.

    Product
    WINNEBAGO — WINNEBAGO VOYAGE!, MICRO MINNIE, MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V154000·2022-03-14

    2021–2022 Dodge Durango and Jeep Grand Cherokee Steering Recall

    Chrysler is recalling 2021–2022 Dodge Durango and 2022 Jeep Grand Cherokee vehicles due to steering gear defect. The rack bar may have been insufficiently hardened, potentially causing loss of steering control.

    Product
    JEEP — JEEP, DODGE GRAND CHEROKEE 4XE, DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V155000·2022-03-14

    2020 Audi S7 and Related Models: Fuel Gauge Malfunction Recall

    Volkswagen Group (Audi) is recalling certain 2019-2022 A6, A7, S6, S7, RS6 Avant, and RS7 vehicles because the fuel level sender may stick, causing inaccurate fuel gauge readings that could lead to engine stalls and crash risk.

    Product
    AUDI — AUDI A6, A7, A6 ALLROAD, S7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V153000·2022-03-11

    Thomas Built Buses Recalls Saf-T-Liner EFX School Buses for Seat Bolt Defect

    Daimler Trucks North America is recalling 2020-2023 Thomas Built Buses Saf-T-Liner EFX school buses because passenger seat mounting bolts may break, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E018000·2022-03-11

    Norco Frames Recalled for Improperly Welded Couplers

    Norco Industries is recalling certain frames with Model CA-5400 couplers due to improper welding that may cause trailer separation.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V150000·2022-03-11

    Ford Recalls F-150, Expedition, Navigator for Brake Master Cylinder Leak

    Ford is recalling 2016-2018 F-150, 2016-2017 Expedition, and Navigator vehicles because a brake master cylinder leak may reduce front brake function and increase crash risk.

    Product
    FORD — FORD, LINCOLN F-150, EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V143000·2022-03-11

    Forest River 2022 Travel Trailers Recalled for Coupler Weld Defect

    Forest River is recalling certain 2022 travel trailers due to improperly welded couplers that may cause trailer separation from the tow vehicle. Dealers will replace the coupler at no charge.

    Product
    FOREST RIVER — FOREST RIVER, EAST TO WEST XLR TOYHAULER, SILVER LAKE, VIBE, DELLA TERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V145000·2022-03-11

    2020-2022 Ford F-59 Steering Shaft Bolt May Loosen, Increasing Crash Risk

    The bolt securing the intermediate steering shaft to the steering gear box may become loose, potentially causing loss of steering control and increased crash risk. Ford is replacing the bolts for free.

    Product
    FORD — FORD F-59
    Category
    Vehicle
    Distribution
    Distributed nationwide