The Recall Desk

State

Connecticut product recalls

20,308 recalls have nationwide distribution and so reach Connecticut. 0 additional recalls listed Connecticut specifically in their distribution scope.

About recalls in Connecticut

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 Connecticut 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.

11851–11875 of 20308

  • HighNHTSA·23V059000·2023-09-02

    RAM 1500 and 2500 Rearview Display May Fail When in Reverse

    Certain 2021-2023 RAM 1500 and 2023 RAM 2500 vehicles have a software defect that may prevent the rearview image from displaying when in reverse, reducing driver visibility.

    Product
    RAM — 2022 RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V060000·2023-09-02

    RAM pickup and cab chassis trucks recalled for engine compartment fire risk

    Chrysler is recalling 2021–2023 RAM 2500, 3500, 4500, and 5500 Cummins diesel trucks due to an electrical short in the heater grid relay that can cause engine compartment fires. Owners should park outside and away from structures until repairs are completed.

    Product
    RAM — 2023 RAM 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V058000·2023-09-02

    2022 Jeep Compass instrument panel display insufficient illumination during daytime

    The 2022 Jeep Compass instrument panel center cluster display may be insufficiently illuminated and may not be visible during daytime driving. This could prevent drivers from seeing safety-critical information like the fuel gauge and warning lights.

    Product
    JEEP — 2022 JEEP COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V061000·2023-09-02

    Motorhome Cooktops May Leak Gas and Create Fire Risk

    Forest River is recalling certain 2022-2023 Coachmen motorhomes with faulty cooktops. The burner tubes may fracture and leak gas, creating a fire hazard.

    Product
    COACHMEN — 2023 COACHMEN GALLERIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V062000·2023-09-02

    Spartan Motorhome Chassis Software Error Causes Loss of Drive Power and Visibility

    Shyft Group is recalling 2022–2024 Spartan motorhome chassis due to a software error that may cause loss of drive power or safety functions like headlights and wipers. Owners should contact Shyft Group at 1-800-237-7806 for a free software update.

    Product
    SPARTAN — 2023 SPARTAN K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V064000·2023-09-02

    2023 Subaru Solterra: hub bolts may loosen and cause wheels to detach

    Certain 2023 Subaru Solterra vehicles have improperly tightened hub bolts that may loosen and cause wheel detachment. Owners should not drive until dealers complete repairs.

    Product
    SUBARU — 2023 SUBARU SOLTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23269·2023-08-31

    Frigidaire Gas Cooktops Recalled for Gas Leak and Fire Hazard

    Electrolux Group is recalling about 215 Frigidaire gas cooktops because plastic control knobs with black shafts can crack or break during use, creating a risk of gas leak and fire. Electrolux has received 63 reports of cracking or breaking, including one minor injury from a gas leak and one report of fire.

    Product
    Frigidaire Stainless-Steel 30-inch 4 Burner and 36-inch 5 Burner Gas Cooktops
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23788·2023-08-31

    Polaris MATRYX PRO RMK and MATRYX RMK KHAOS Snowmobiles Recalled for Puncture Hazard

    Polaris is recalling about 15,900 Model Year 2022–2023 MATRYX PRO RMK and MATRYX RMK KHAOS snowmobiles because handlebar hooks pose a puncture hazard and risk of serious injury during crashes. The firm has received four reports of puncture wounds.

    Product
    Polaris Snowmobiles, Model Year 2022-2023 MATRYX PRO RMK and MATRYX RMK KHAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23787·2023-08-31

    Chemboys DIYChemicals Potassium and Sodium Hydroxide Lacks Child-Resistant Packaging

    Chemboys is recalling DIYChemicals potassium hydroxide and sodium hydroxide products because the packaging is not child-resistant and labels lack mandatory hazard information. The products pose a risk of chemical burns and eye irritation to children.

    Product
    DIYChemicals: Potassium Hydroxide/KOH Flakes and Sodium Hydroxide
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23786·2023-08-31

    Ski-Doo and Lynx Snowmobiles Recalled for Fire Hazard

    Bombardier Recreational Products is recalling about 4,070 model year 2023 Ski-Doo and Lynx snowmobiles equipped with 850 E-TEC Turbo R engines because the main injector fuel return hose can leak, posing a fire hazard.

    Product
    Ski-Doo and Lynx Snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23271·2023-08-31

    Prime-Line Recalls Glass Doorknobs Due to Laceration Hazard

    Prime-Line glass doorknobs can crack and separate, creating a laceration hazard. The firm has received five reports of injuries requiring stitches.

    Product
    Glass Doorknobs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23272·2023-08-31

    Boon Flair and Flair Elite Highchairs Recalled for Fall Hazard

    TOMY International is recalling about 83,000 Boon Flair and Flair Elite highchairs because loose bolts can allow the seat to detach from the base, creating a fall hazard. The company has received 34 reports of separation, including 24 falls with 11 injuries.

    Product
    Boon Flair & Flair Elite highchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23270·2023-08-31

    Apollo Phantom Electric Scooters Recalled for Fall and Injury Hazards

    Apollo Imports Inc. is recalling approximately 3,900 Apollo Phantom Electric Scooters because a stem bolt can come loose, causing the suspension and wheel assembly to separate and posing a fall and injury hazard. The company has received seven reports of bolt breaking, including three injuries.

    Product
    Apollo Phantom Electric Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2248-2023·2023-08-30

    Carina Sub-Acute Care Ventilator Recalled for Toxic Chemical Emission

    Draeger Medical is recalling 11,621 Carina Sub-Acute Care Ventilators because polyurethane components emit 1,3-Dichloropropan-2-ol at levels exceeding safe limits during extended use in pediatric patients.

    Product
    Carina Sub-Acute Care Ventilator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2455-2023·2023-08-30

    IMPIX DLIF Intervertebral Fusion Device Recalled for Packaging Defect

    Medicrea International is recalling IMPIX DLIF intervertebral fusion devices due to potential pinholes in product packaging that could compromise sterility.

    Product
    IMPIX DLIF, REF numbers: a) B16123509, b) B16123511, c) B16124009, d) B16124013, e) B16124509, f) B16124511, g) B16124513, h) B16164009, i) B16164013, j) B16165009, k) B16165013; intervertebral fusion device - lumbar
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1101-2023·2023-08-30

    FDA Recalls AstrinGyn Surgical Hemostatic Due to Manufacturing Practice Deviations

    Ecometics is recalling 92,967 vials of AstrinGyn (Ferric Subsulfate) Aqueous due to manufacturing practice violations. The product was not manufactured under current good manufacturing practices (CGMP).

    Product
    AstrinGyn (Ferric Subsulfate) Aqueous, 259 mg/g, 8 gm Single Use Vials, Manufactured for CooperSurgical, Trumbull, CT 06611, NDC 59365-6065-0, Ref 6065.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2445-2023·2023-08-30

    Dolomite Gloss Rollator Structural Failure Recall: Seat Collapse Risk

    Dolomite Gloss Rollator models may experience seat failure and structural collapse due to broken eyelets and crossbar, potentially causing user injury. About 586 units nationwide are affected.

    Product
    DOLOMITE GLOSS ROLLATOR - intended to support during walking and may also serve as a resting seat. Model Number(s): 1654807 - DOLOMITE GLOSS 680 ROLLATOR 1655081 - DOLOMITE GLOSS 600 ROLLATOR 1655082 - DOLOMITE GLOSS 520 ROLLATOR 1655083 - DOLOMITE GLOSS 450 ROLLATOR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2446-2023·2023-08-30

    Randox Liquid Urine Control Level 2 Recalled for Analytical Accuracy Issues

    Randox Liquid Urine Control Level 2 (Lot 1209UC) is recalled for incorrect hCG and cortisol values and a transcription error in instructions. The defects may delay patient test reporting.

    Product
    Randox Liquid Urine Control Level 2- intended for in vitro diagnostic use, in the quality control of Amylase, Calcium, Chloride, Cortisol, Creatinine, Glucose, hCG pregnancy, Magnesium, Microalbumin, Osmolality, pH, Phosphate Inorganic, Potassium, Protein Total, Sodium, Specific
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2447-2023·2023-08-30

    Air/Water Valve Used with Olympus Endoscopes May Malfunction

    Olympus air/water valves used with ultrasonic endoscopes may fail during automated reprocessing, potentially allowing body fluids to backflow into the air channel. Approximately 29,590 units nationwide are affected.

    Product
    The Air/Water Valve is provided/used with the following Endoscopes: ULTRASONIC GASTROFIBERSCOPE, ULTRASONIC GASTROVIDEOSCOPE, ULTRASONIC COLONOVIDEOSCOPE: GF-UC140P-AL5, GF-UCT140-AL5, GF-UE160-AL5, GF-UCT180, GF-UM20, GF-UM130, GF-UMQ130, GF-UM160, GF-UC160P-OL5, GF-UCT160-OL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1105-2023·2023-08-30

    Compounded Semaglutide/Cyanocobalamin Vials Recalled for Sterility Concerns

    Tailor Made Compounding is recalling 9 vials of Semaglutide/Cyanocobalamin 2mg/0.4mg/mL due to inability to assure sterility. The product was distributed nationwide.

    Product
    Semaglutide/Cyanocobalamin 2mg/0.4mg/mL, 1mLvials, Tailor Made Compounding.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2459-2023·2023-08-30

    Medicrea GRANVIA-C Cervical Fusion Device Recalled for Packaging Defects

    Medicrea International is recalling GRANVIA-C cervical intervertebral fusion devices due to a packaging non-conformity issue presenting as pinholes in inner or outer pouches, which could compromise sterility.

    Product
    GRANVIA-C, REF numbers: a)¿¿¿¿¿ A13111427, b)¿¿¿¿ A13112567, c)¿¿¿¿¿ A13113456, d)¿¿¿¿ A13131516, e)¿¿¿¿ A13131789, f)¿¿¿¿¿¿ A13132012, g)¿¿¿¿¿ B13111014, h)¿¿¿¿ B13111015, i)¿¿¿¿¿¿ B13111016, j)¿¿¿¿¿¿ B13111017, k)¿¿¿¿¿ B13111025, l)¿¿¿¿¿¿ B13111026, m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1102-2023·2023-08-30

    Lugol's Strong Iodine Solution Recalled Due to Manufacturing Quality Deviations

    Ecometics, Inc. is recalling Lugol's Strong Iodine Solution nationwide due to manufacturing quality deviations. Consumers with affected prescription vials should consult their healthcare provider.

    Product
    Lugol's (Strong Iodine Solution USP), Each mL contains Iodine 0.05gm and potassium iodide 0.100gm, 8mL Single Use Vials, Rx Only, Manufactured for CooperSurgical, Trumbull, CT 06611, NDC 59365-6064-0, Ref 6064.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1457-2023·2023-08-30

    Butter Flavored Popcorn recalled for undeclared milk

    Bickel's Snack Foods Inc is recalling Butter Flavored Popcorn because the product contains undeclared milk. The recall affects approximately 6,048 bags distributed in Georgia and nationwide retail stores.

    Product
    Butter Flavored Popcorn Naturally & Artificially Flavored, 8oz. UPC: 70175 06021 Packaged in clear plastic bags, 9 bags per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2462-2023·2023-08-30

    Medicrea IMPIX MANTA+ Cervical Fusion Devices Recalled for Packaging Defect

    Medicrea International is recalling IMPIX MANTA+ cervical intervertebral fusion devices due to potential packaging non-conformity with pinholes in inner or outer pouches. No illnesses or injuries reported.

    Product
    IMPIX MANTA+, REF numbers: a) B20171743, b) B20171753, c) B20171763, d) B20171773, e) B20171943, f) B20171953, g) B20171963, h) B20171973, i) B20172253, j) B20172263, k) B20172273; intervertebral fusion device - cervical
    Category
    Medical Device
    Distribution
    Distributed nationwide