The Recall Desk

State

Connecticut product recalls

72,820 recalls have nationwide distribution and so reach Connecticut. 6,564 additional recalls listed Connecticut specifically in their distribution scope.

What the numbers show

Total
6,564
Critical
838
Severe
1,586
Most recent
2026-09-02

Of the 6,564 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 1,586 (24%) are Severe.

Which agencies issued them

These figures cover only the 6,564 recalls whose distribution notice names Connecticut specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

626–650 of 79384

  • SevereFDA (Devices)·Z-2692-2026·2026-07-22

    ABIOMED Insertion Kit heart pump accessories introducer sheath leakage

    Abiomed is recalling ABIOMED Insertion Kits due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable by users.

    Product
    ABIOMED Insertion Kit, Pkgd, JP, Pump Set Code 0052-0011-JP; containing Introducer Product Code 0052-3006-JP. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1158-2026·2026-07-22

    D'Dioses Coconut Ice Pop Recall Due to Undeclared Allergens

    D'Dioses Coconut Ice Pops (4 oz) may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these substances should not consume the product.

    Product
    Ice Pop, D'Dioses Coconut, 4 oz (85 g), with UPC 710594511867
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2705-2026·2026-07-22

    One-Piece Introducer Tray kits recalled for sterility failure

    Argon Medical Devices is recalling One-Piece Introducer Tray kits containing Lidocaine HCL Injection because they do not meet sterility release criteria. The kits were distributed nationwide and internationally.

    Product
    One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2690-2026·2026-07-22

    Abiomed Impella CP Smart Assist Set Heart Pump Introducer Sheath Leakage

    Abiomed is recalling the Impella CP Smart Assist Set due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines in 14Fr and 23Fr introducers. These manufacturing issues are not visually detectable.

    Product
    ABIOMED Impella CP Smart Assist Set, JP, Pump Set Code 0048-0024-JP; containing Introducer Product Code 0052-3025-JP. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1162-2026·2026-07-22

    Ice Pop D'Dioses Guayaba recalled for undeclared allergens

    D'Dioses Fruit Pops, Inc. is recalling D'Dioses Guayaba ice pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these ingredients should not consume the product.

    Product
    Ice Pop, D'Dioses Guayaba, 1 Bar (81.7 g), with UPC 827912008432
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2720-2026·2026-07-22

    Olympus Ellik Evacuator Recalled for Inadequate Sterilization Risk

    Olympus Corporation of the Americas is recalling the Olympus Ellik Evacuator (Model 194) worldwide because certain sterilization parameters in the instructions may not render the device adequately sterile.

    Product
    Olympus Ellik Evacuator Includes Glass Body, Male Connecting Tubing & Latex Bulb. Model Number: 194.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1170-2026·2026-07-22

    D'Dioses Grocella Ice Pop Recalled for Undeclared Allergens

    D'Dioses Fruit Pops, Inc. is recalling D'Dioses Grocella Ice Pop (1 bar, 81.7 g) due to undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in NJ, CT, NY, and PA.

    Product
    Ice Pop, D'Dioses Grocella, 1 Bar (81.7 g), with UPC 827912008531
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2723-2026·2026-07-22

    ICU Medical Plum Duo Infusion Pump Software Defect Affecting Drug Delivery

    ICU Medical is recalling Plum Duo Infusion Pump v1.2.3 units due to a software defect that may cause the pump to deliver up to twice the programmed volume without decrementing the display, risking patient overdose.

    Product
    ICU Medical Plum Duo Infusion Pump, v1.2.3: 1) Item Number 400020401 and 2) Item Number 400020403; infusion pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1166-2026·2026-07-22

    Ice Pop, D'Dioses Nuez, recalled for undeclared allergens

    D'Dioses Fruit Pops, Inc. is recalling D'Dioses Nuez Ice Pop bars because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40, which pose a serious health risk to consumers with allergies or sensitivities.

    Product
    Ice Pop, D'Dioses Nuez, 1 Bar (81.7 g), with UPC 827912008548
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2708-2026·2026-07-22

    Arterial Line Kit with Lidocaine HCL Injection Fails Sterility Testing

    Argon Medical Devices is recalling an Arterial Line Kit containing Lidocaine HCL Injection USP because the kits do not meet sterility release criteria, creating a risk of infection from non-sterile medical injection.

    Product
    Arterial Line Kit 20ga x 6, REF: 400115A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2686-2026·2026-07-22

    ABIOMED Impella CP Introducer Kit 14 Fr potentially defective sheath

    Abiomed, Inc. is recalling ABIOMED Impella CP Introducer Kit 14 Fr units worldwide due to potential introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable.

    Product
    ABIOMED Impella CP Introducer Kit 14 Fr, 25 cm, Pump Set Code 0052-0039, containing Kit, 14Fr Introducer, 25cm, Long Taper, Introducer Product Code 0052-3053. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2709-2026·2026-07-22

    Bone Marrow Tray kits recalled due to sterility failure

    Argon Medical Devices is recalling Bone Marrow Tray kits containing Lidocaine HCL Injection because they do not meet sterility release criteria.

    Product
    Bone Marrow Tray, REF: CB0033TL; CB0355TLA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2682-2026·2026-07-22

    ABIOMED Impella CP Heart Pump Introducer Sheath Leakage Risk

    Abiomed is recalling the Impella CP heart pump set (87,277 units worldwide) due to potential leakage from the introducer sheath that cannot be visually detected by users. The defect affects the 14Fr and 23Fr introducers included in every pump set.

    Product
    ABIOMED Impella CP Set, Pump Set Code 0048-0003, containing BIOMED Impella Introducer, 14 Fr, 13 cm & 25 cm, Product Code 0052-3046. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2683-2026·2026-07-22

    ABIOMED Impella CP Introducer Kit 14Fr heart pump safety recall

    ABIOMED Impella CP Introducer Kit 14Fr is being recalled due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines. The manufacturing defect is not visually detectable by users.

    Product
    ABIOMED Impella CP Introducer Kit 14 Fr, 13 and 25 cm, Pump Set Code 1000550, containing Kit, 14Fr Introducer, 13cm&25cm, Sterile, Introducer Product Code 0052-3046. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2685-2026·2026-07-22

    Abiomed Impella CP Introducer Kit heart pump accessory recall

    Abiomed is recalling Impella CP Introducer Kits worldwide due to potential leakage from the introducer sheath that cannot be visually detected by users. The manufacturing defect affects 1,540 units across multiple countries.

    Product
    ABIOMED Impella CP Introducer Kit 14 Fr, 13 cm, Pump Set Code 0052-0038, containing Kit, 14Fr Introducer, 13cm, Long Taper, Introducer Product Code 0052-3052. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1171-2026·2026-07-22

    D'Dioses Mango Ice Pops Recalled for Undeclared Allergens

    D'Dioses Mango Ice Pops (3.7 oz) are being recalled because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these ingredients should not consume the product.

    Product
    Ice Pop, D'Dioses Mango, 3.7 oz (81.7 g), with UPC 827912008494
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2687-2026·2026-07-22

    ABIOMED Impella 5.5 Heart Pump Introducer Sheath Leakage Risk Recall

    Abiomed is recalling the Impella 5.5 Smart Assist Set heart pump due to potential leakage from introducer sheaths. The defect is not visually detectable and affects all affected pump sets worldwide.

    Product
    ABIOMED Impella 5.5 Smart Assist Set, JP, Pump Set Codes 1000211, 1000212; containing Introducer Product Code 0052-3006-JP. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0689-2026·2026-07-22

    Cleviprex Injectable Emulsion Recall Due to Sterility Assurance Concerns

    Chiesi USA, Inc. is recalling Cleviprex (clevidipine) injectable emulsion due to lack of assurance of sterility. The affected product is distributed nationwide.

    Product
    CLEVIPREX — CLEVIPREX (CLEVIPIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2684-2026·2026-07-22

    ABIOMED Introducer Kit 23 Fr heart pump accessory leakage risk

    Abiomed is recalling ABIOMED Introducer Kit 23 Fr due to potential sheath leakage from manufacturing defects. The leakage risk is not visually detectable and affects all current batches worldwide.

    Product
    ABIOMED Introducer Kit 23 Fr, 11 cm, Pump Set Code 1000441, containing Kit, 23Fr Introducer, 11cm, Sterile, Introducer Product Code 2000342. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1169-2026·2026-07-22

    Ice Pop D'Dioses Limon recalled for undeclared allergens

    D'Dioses Fruit Pops, Inc. is recalling Ice Pop D'Dioses Limon 4 oz packages because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies or sensitivities to these ingredients should not consume the product.

    Product
    Ice Pop, D'Dioses Limon, 4 oz (85 g), with UPC 710594511836
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·H-1173-2026·2026-07-22

    Ice Pop D'Dioses Nanche Recalled for Undeclared Allergens

    D'Dioses Fruit Pops, Inc. is recalling D'Dioses Nanche ice pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. The product was distributed in NJ, CT, NY, and PA.

    Product
    Ice Pop, D'Dioses Nanche, 1 Bar (81.7 g), with UPC 827912008449
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·H-1163-2026·2026-07-22

    Ice Pop D'Dioses Vainilla Recalled for Undeclared Allergens

    D'Dioses Fruit Pops, Inc. is recalling D'Dioses Vainilla ice pops because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. The products were distributed in NJ, CT, NY, and PA.

    Product
    Ice Pop, D'Dioses Vainilla, 4 oz (85 g), with UPC 710594511829
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2689-2026·2026-07-22

    ABIOMED Impella CP Heart Pump Set Introducer Sheath Leakage Risk

    ABIOMED is recalling Impella CP heart pump sets worldwide due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines in 14Fr and 23Fr introducers. The manufacturing defect is not visually detectable.

    Product
    ABIOMED Impella CP Set, Pump Set Code 0048-0014; containing Introducer Product Code 0052-3046. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0690-2026·2026-07-22

    ChloraPrep One-Step Applicators Recalled for Potential Packaging Seal Defects

    CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) applicators nationwide because affected units may have open or incomplete seals on the packaging, which could compromise sterility assurance.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1159-2026·2026-07-22

    D'Dioses Fresa Leche Ice Pop Recalled for Undeclared Allergens

    D'Dioses Fresa Leche ice pops may contain undeclared milk, pecans, pistachios, and food colorings (yellow #5 and red #40). The product was distributed in NJ, CT, NY, and PA.

    Product
    Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), with UPC 710594511850
    Category
    Food
    Distribution
    4 states