The Recall Desk

State

Maine product recalls

72,820 recalls have nationwide distribution and so reach Maine. 3,894 additional recalls listed Maine specifically in their distribution scope.

What the numbers show

Total
3,894
Critical
468
Severe
791
Most recent
2026-09-02

Of the 3,894 recalls naming Maine we have scored against our rubric, 468 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 791 (20%) are Severe.

Which agencies issued them

These figures cover only the 3,894 recalls whose distribution notice names Maine specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

601–625 of 76714

  • 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 (Devices)·Z-2681-2026·2026-07-22

    ABIOMED Impella RP Flex heart pump introducer sheath leakage risk

    Abiomed is recalling the Impella RP Flex heart pump due to potential introducer sheath leakage from the sheath cap and hub score lines. The manufacturing defect is not visually detectable.

    Product
    ABIOMED Impella RP Flex with SmartAssist Set, Pump Set Code 1000323, containing Kit, 23Fr Introducer, 11cm, Sterile, 23 Fr, 11 cm, Product Code 2000342. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2704-2026·2026-07-22

    Transvenous Pacing Electrode Tray with Bipolar Balloon Pacing Electrode Recalled

    Argon Medical Devices is recalling Transvenous Pacing Electrode Trays with Bipolar Balloon Pacing Electrode 5F because kits containing Lidocaine HCL Injection USP did not meet sterility release criteria.

    Product
    Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 008566A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2693-2026·2026-07-22

    ABIOMED Intro Kit Heart Pump Introducer Sheath Leakage Risk

    Abiomed, Inc. is recalling ABIOMED Intro Kit heart pump introducer sheaths due to potential leakage from under the sheath cap and along hub score lines. The manufacturing defects are not visually detectable by users.

    Product
    ABIOMED Intro Kit, 14Fr x 13 and 25 cm, PKGD, JP, Pump Set Code 0052-0023-JP; containing Introducer Product Code 0052-3025-JP. heart pump and accessories
    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 (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-2739-2026·2026-07-22

    Medtronic Bio-Medicus Adult Cannula Kit Recalled for Foreign Material

    Medtronic is recalling its Bio-Medicus Adult Cannula Kit (Product Number 96530-115) used in cardiopulmonary bypass procedures due to the discovery of loose foreign material containing trace levels of blood in two units.

    Product
    Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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 (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-2688-2026·2026-07-22

    Abiomed Impella 5.5 SmartAssist S2 heart pump introducer sheath leakage risk

    Abiomed is recalling Impella 5.5 SmartAssist S2 heart pump sets worldwide due to a potential for introducer sheath leakage from under the sheath cap and along hub score lines that may not be visible to users.

    Product
    ABIOMED Impella 5.5 SmartAssist S2 Set, JP, Pump Set Codes 1000459, 1000460; containing Introducer Product Code 0052-3006-JP. heart pump and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2724-2026·2026-07-22

    ICU Medical Plum Solo Precision IV Pump May Deliver Excess Medication

    ICU Medical is recalling the Plum Solo Precision IV Pump (v1.0.3) because in specific scenarios, the pump may fail to decrease the displayed volume and could deliver up to twice the programmed medication amount.

    Product
    ICU Medical Plum Solo Precision IV Pump, v1.0.3, Item Number 400010401; infusion pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V471000·2026-07-22

    ATC Recalls 2026 RM500 and RM700 Trailers Due to Winch Remote Issue

    Aluminum Trailer Company is recalling 2026 RM500 and RM700 trailers because the wireless remote may cause unexpected winch movements, increasing injury risk.

    Product
    ATC — ATC RM500, RM700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V475000·2026-07-22

    Freightliner Trucks Recalled for Low Beam Headlight Software Error

    Daimler Trucks North America is recalling 2026-2027 Freightliner models because a software error may cause low beam headlights to illuminate improperly, increasing crash risk.

    Product
    FCCC — FCCC, FREIGHTLINER S2C, S2RV, BUSINESS CLASS M2, EM2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2718-2026·2026-07-22

    Olympus Toomey Evacuator 30cc medical device sterilization parameters recalled

    Olympus Corporation recalled the Toomey Evacuator 30cc with Adaptor (Model 188) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.

    Product
    Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1154-2026·2026-07-22

    Pillsbury Bread Rolls Hard Roll Dough Recalled for Glass

    General Mills is recalling Pillsbury Bread Rolls Hard Roll Dough due to potential glass contamination. Affected products were distributed across multiple states.

    Product
    Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4. Case UPC 107-21582-13283-1. Keep Frozen. Case Qty 180. Distributed by: General Mills Sales, Inc. Minneapolis, MN 55440.
    Category
    Food
    Distribution
    19 states
  • HighFDA (Devices)·Z-2738-2026·2026-07-22

    Medtronic DLP One-Piece Pediatric Arterial Cannula Recalled for Foreign Material

    Medtronic is recalling certain DLP One-Piece Pediatric Arterial Cannulas (Product Number 77010) due to complaints of loose foreign material containing trace levels of blood found in the devices.

    Product
    Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2727-2026·2026-07-22

    GE Optima XR200/220/240amx Radiographic System Column Safety Mechanism

    GE Medical Systems is recalling certain Optima XR200/220/240amx mobile radiographic systems after column replacements because functional testing of the safety pawl may not have been performed, which could allow the X-ray arm to drop and injure patients.

    Product
    Optima XR220amx, Mobile Digital-Ready Radiographic System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2726-2026·2026-07-22

    GE Medical Optima XR200/220/240amx Mobile Radiographic Systems Recall

    GE HealthCare recalls certain Optima XR200/220/240amx mobile radiographic systems where safety testing may have been incomplete after column replacement. A failed counterpoise cable could cause the X-ray arm to drop on patients.

    Product
    Optima XR200amx, Mobile Digital-Ready Radiographic System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2719-2026·2026-07-22

    Olympus Toomey Evacuator 50cc with Adaptor sterilization recall

    Olympus is recalling the Toomey Evacuator 50cc with Adaptor (Model 188A) because some sterilization parameters in the instructions may not reliably render the devices sterile.

    Product
    Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2721-2026·2026-07-22

    Olympus Glass Body for 194 Ellik Evacuator Model 190A Sterilization Recall

    Olympus Corporation is recalling the Glass Body for 194 Ellik Evacuator (Model 190A) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.

    Product
    Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1155-2026·2026-07-22

    Pillsbury Kaiser Roll Dough recalled for potential glass contamination

    General Mills is recalling Pillsbury Bread Rolls, Kaiser Roll Dough due to potential foreign glass material in the product. Affected consumers should not consume the product and should contact the company or retailer for a refund.

    Product
    Pillsbury Bread Rolls, Kaiser Roll Dough. 144 units / 2.5oz each. Net Wt. 22.5 lb (10.2kg) Package UPC 7 21582-13288 9. Case UPC 107-21582-13288-6. Keep Frozen. Case Qty 144. Distributed by: General Mills Sales, Inc. Minneapolis, MN 55440.
    Category
    Food
    Distribution
    19 states
  • HighNHTSA·26V472000·2026-07-22

    Coach and Equipment Recalls Phoenix and Metrolite Buses with Lift Defect

    Coach and Equipment is recalling 2024-2026 Phoenix and Metrolite buses because a wheelchair lift may fail to stop, increasing injury risk.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT METROLITE, PHOENIX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E047000·2026-07-22

    Hiab Recalls K-HiPro Cranes Due to Potential Column Weld Failure

    Hiab USA Inc. is recalling K-HiPro 425 and 505 cranes because a weld may crack, risking column collapse and injury.

    Product
    EQUIPMENT:MECHANICAL:BOOM/CRANE/LADDER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2725-2026·2026-07-22

    Rapid Refill Continuous Injection System Recalled for Syringe Loosening Risk

    Boston Scientific's Rapid Refill Continuous Injection System (UPN M00566001) is being recalled because the recalled Medline Namic Angiographic Control Syringe may loosen or disconnect from the manifold, potentially causing leakage, inability to aspirate or inject, and procedure delays.

    Product
    Rapid Refill Continuous Injection System, UPN M00566001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2741-2026·2026-07-22

    Vasoview Hemopro 2 Endoscopic Vessel Harvesting System Recall

    Maquet Cardiovascular is recalling Vasoview Hemopro 2 devices from Lot 3000547797 due to exposure to out-of-specification sterilization during gamma sterilization. The affected devices may not be properly sterilized.

    Product
    The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.
    Category
    Medical Device
    Distribution
    Distributed nationwide