The Recall Desk

State

Connecticut product recalls

72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3001–3025 of 79502

  • ModerateFDA (Drugs)·D-0366-2026·2026-03-11

    Med-Nap BZK antiseptic towelettes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Med Nap BZK Antiseptic Towelettes in 100-count packs over current good manufacturing practice deviations.

    Product
    MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC — MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0383-2026·2026-03-11

    Midodrine hydrochloride tablets recalled over inadequately sealed blister packaging

    The Harvard Drug Group is recalling one lot of Midodrine Hydrochloride Tablets 5 mg because of a defective container with inadequately sealed blister packaging.

    Product
    MIDODRINE HYDROCHLORIDE — MIDODRINE HYDROCHLORIDE (MIDODRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0387-2026·2026-03-11

    Zone 2 lidocaine cream recalled because stability data does not support expiry

    HTO Nevada, trading as Kirkman, is recalling one lot of Maximum Zone 2 4% Lidocaine Cream because the stability data does not support the labeled expiry date.

    Product
    MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-015.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0370-2026·2026-03-11

    Med-Nap cleansing towelette bulk packs recalled over manufacturing deviations

    Acme United Corporation is recalling Med-Nap Cleansing Towelettes in bulk cases over current good manufacturing practice deviations.

    Product
    MED NAP CLEANSING TOWELETTE — MED NAP CLEANSING TOWELETTE (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0358-2026·2026-03-11

    First Aid Only BZK antiseptic wipes recalled over manufacturing deviations

    Acme United Corporation is recalling First Aid Only BZK Antiseptic Towelettes in 100-count packs over current good manufacturing practice deviations.

    Product
    FIRST AID ONLY BZK ANTISEPTIC — FIRST AID ONLY BZK ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0382-2026·2026-03-11

    Nilotinib 200 mg capsules recalled after failing appearance tests

    Cipla USA is recalling one lot of Nilotinib Capsules 200 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.

    Product
    NILOTINIB — NILOTINIB (NILOTINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0381-2026·2026-03-11

    Nilotinib capsules recalled after failing appearance tests at six months

    Cipla USA is recalling three lots of Nilotinib Capsules 150 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.

    Product
    NILOTINIB — NILOTINIB (NILOTINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V135000·2026-03-06

    2026 Kia K4 vehicles recalled for defective rear seat belt anchor

    Kia is recalling certain 2026 K4 vehicles because the rear center seat belt anchor buckle may not latch properly, risking occupant restraint failure in a crash.

    Product
    KIA — KIA K4, TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V134000·2026-03-06

    Mercedes-Benz Recalls 2026 GLA 250 for Door Latch Defect

    Mercedes-Benz is recalling 2026 GLA 250 vehicles because an incorrectly installed bowden cable may prevent the door from opening from inside, potentially trapping occupants.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V128000·2026-03-05

    Toyota Highlander second-row seat backs may fail to lock

    Toyota is recalling certain 2021-2024 Highlander and Highlander Hybrid vehicles because the second-row seat backs may fail to lock into position during seat back adjustment.

    Product
    TOYOTA — TOYOTA HIGHLANDER HYBRID, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V129000·2026-03-05

    GM heavy duty pickup fuel pump may cause an engine stall

    GM is recalling certain 2025-2026 Chevrolet Silverado 3500 and GMC Sierra 3500 vehicles with gasoline engines and dual fuel tanks because the rear fuel pump may not transfer adequate fuel to the front tank.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 3500, SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V131000·2026-03-05

    Forest River Recalls 2026 Dynamax Motorhomes Due to Electrical Bonding Defect

    Forest River is recalling 2026 Dynamax Europa and Grand Sport GT motorhomes because the distribution panel may not be properly bonded to the chassis ground, posing a risk of injury or electrocution.

    Product
    DYNAMAX — DYNAMAX GRAND SPORT GT, EUROPA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V126000·2026-03-05

    Mitsubishi Fuso Rizon Trucks Recalled for Electrical Control Unit Error

    Mitsubishi Fuso is recalling 2024-2025 Rizon trucks because an electrical control unit error may prevent the vehicle from moving, increasing crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO RIZON FEC7K (E16), RIZON FEC9K (E18), RIZON FECXK (E18)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26312·2026-03-05

    Minoxidil hair regrowth spray recalled for lacking child-resistant packaging

    Tomum Minoxidil Hair Growth Treatment spray bottles are being recalled because the bottles are not child-resistant, as required for minoxidil under the Poison Prevention Packaging Act.

    Product
    Tomum Hair Regrowth Treatment with Minoxidil for Men and Women Spray Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V127000·2026-03-05

    GM Recalls 2025-2026 Chevrolet Express and GMC Savana for Tire Damage

    General Motors is recalling 2025-2026 Chevrolet Express and GMC Savana cutaway vehicles because tires may have sidewall damage, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26317·2026-03-05

    Building block sets recalled because button cell batteries are accessible

    Cubimana Island Storm 3 In 1 Building Sets are being recalled because the battery compartment in the LED light piece lets children access button cell batteries.

    Product
    Cubimana Island Storm 3 In 1 Building Sets with LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26315·2026-03-05

    HALO Magic Sleepsuits recalled because zipper heads can detach

    HALO Magic Sleepsuits in three batch codes are being recalled because the zipper head can detach from the garment, posing a choking hazard to infants.

    Product
    HALO Magic Sleepsuits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V130000·2026-03-05

    Forest River Recalls 2026 Impression Trailers Due to Wiring Defect

    Forest River is recalling 2026 Impression fifth wheel trailers because exposed wire conductors may cause electrical arcing and increase fire risk.

    Product
    FOREST RIVER — FOREST RIVER IMPRESSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0350-2026·2026-03-04

    Fluorescein Sodium Ophthalmic Strips Recalled Over Sterility Concerns

    Wizcure Pharmaa is recalling all lots of Fluorescein Sodium Ophthalmic Strips because the products may not have been manufactured according to current good manufacturing practices, raising concerns about sterility assurance.

    Product
    C20H10NA2O5 FLUORESCEIN SODIUM OPHTHALMIC STRIPS — C20H10NA2O5 FLUORESCEIN SODIUM OPHTHALMIC STRIPS (FLUORESCEIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1459-2026·2026-03-04

    Knee and Humeral Socket Implants Recalled for Incorrect Labeling

    Encore Medical, LP is recalling 14 EMPOWR 3D KNEE implants because they contain incorrect labeling. The recall affects US nationwide distribution.

    Product
    Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707
    Category
    Medical Device
    Distribution
    Distributed nationwide