The Recall Desk

State

Connecticut product recalls

72,940 recalls have nationwide distribution and so reach Connecticut. 6,566 additional recalls listed Connecticut specifically in their distribution scope.

What the numbers show

Total
6,566
Critical
838
Severe
1,588
Most recent
2026-09-09

Of the 6,566 recalls naming Connecticut we have scored against our rubric, 838 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,588 (24%) are Severe.

These figures cover only the 6,566 recalls whose distribution notice names Connecticut specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3776–3800 of 79506

  • HighCPSC·26183·2026-01-15

    Energizer lanterns recalled because the lithium-ion battery can overheat

    About 4,100 Energizer Large Power Indicator Lanterns are being recalled because the lithium-ion batteries installed in them can overheat, posing a burn hazard.

    Product
    Energizer® Large Power Indicator Lanterns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V012000·2026-01-15

    Ford engine block heater may crack and short circuit when plugged in

    Ford is recalling certain 2016-2018 Focus, 2019 Explorer and 2024 Explorer vehicles because the engine block heater may crack and develop a coolant leak, causing a short circuit when plugged in.

    Product
    FORD — FORD FOCUS, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26194·2026-01-15

    HEZI power strips recalled over an ungrounded metal enclosure

    About 1,320 HEZI brand power strips are being recalled because they have an ungrounded metal enclosure that poses an electrocution hazard if energized.

    Product
    HEZI Branded Power Strips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26191·2026-01-15

    Crib mattresses recalled because they may not fit certain cribs

    About 1,500 KEAWIS crib mattresses are being recalled because they may not adequately fit certain play yards or non-full-sized cribs, creating gaps that pose an entrapment hazard.

    Product
    KEAWIS Crib Mattress
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26192·2026-01-15

    Adirondack patio chairs recalled because they can crack and collapse

    About 6,100 Adams RealComfort and StyleWell Adirondack patio chairs are being recalled because the chairs can crack and collapse, posing injury and fall hazards.

    Product
    Adams RealComfort and StyleWell Adirondack Patio Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0374-2026·2026-01-14

    Locatelli pecorino romano shippers recalled after testing positive for Listeria

    Ambriola is recalling 184 units of Locatelli Grated Pecorino Romano 48/8oz shippers after the product tested positive for Listeria monocytogenes.

    Product
    Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup & Lid, 48 units per case
    Category
    Food
    Distribution
    20 states
  • CriticalFDA (Drugs)·D-0288-2026·2026-01-14

    ReBoost nasal spray recalled over yeast, mold and microbial contamination

    MediNatura is recalling all lots within expiry of ReBoost Nasal Spray after the products were found to contain yeast, mold and microbial contamination identified as Achromobacter.

    Product
    REBOOST — REBOOST (SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE AND PULSATILLA VULGARIS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1000-2026·2026-01-14

    Organ recovery packs recalled as not suitable for organ transplant

    AVID Medical is recalling 132 Halyard Organ Recovery OR Packs, kit code LLOG1000-15, because the devices are not suitable for organ transplant.

    Product
    Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1001-2026·2026-01-14

    Organ recovery surgical packs recalled as not suitable for organ transplant

    AVID Medical is recalling 52 Halyard Organ Recovery OR Packs because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.

    Product
    Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1002-2026·2026-01-14

    Mini Plus surgical kits recalled as not suitable for organ transplant

    AVID Medical is recalling 380 Halyard Mini Plus Kit South units because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.

    Product
    Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0289-2026·2026-01-14

    ClearLife allergy nasal spray recalled over yeast, mold and microbial contamination

    MediNatura is recalling all lots within expiry of ClearLife Allergy Nasal Spray, Extra Strength, after the products were found to contain yeast, mold and Achromobacter.

    Product
    CLEARLIFE EXTRA STRENGTH — CLEARLIFE EXTRA STRENGTH (ONION, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, SULFUR, AMBROSIA ARTEMISIIFOLIA WHOLE, EUPHRASIA STRICTA AND SCHOENOCAULON OFFICINALE SEED)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0373-2026·2026-01-14

    Ambriola Piccante pecorino romano recalled after testing positive for Listeria

    Ambriola is recalling 179 bags of Ambriola Piccante grated Pecorino Romano in 5 and 10-pound sizes after the product tested positive for Listeria monocytogenes.

    Product
    Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags (units)
    Category
    Food
    Distribution
    20 states
  • CriticalFDA (Food)·H-0372-2026·2026-01-14

    Boar's Head pecorino romano in five pound bags recalled over Listeria

    Ambriola is recalling 405 five-pound bags of Boar's Head Pecorino Romano Grated after the product tested positive for Listeria monocytogenes.

    Product
    Boar's Head Pecorino Romano Grated, 5-pound plastic bag (unit)
    Category
    Food
    Distribution
    20 states