The Recall Desk

State

Maine product recalls

72,919 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.

These figures cover only the 3,894 recalls whose distribution notice names Maine specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2551–2575 of 76813

  • HighFDA (Drugs)·D-0412-2026·2026-04-08

    Leader ultra lubricating eye drops recalled over sterility assurance failure

    Leader Ultra Lubricating Eye Drops, containing polyethylene glycol 400 and propylene glycol, are being recalled for lack of assurance of sterility.

    Product
    LEADER ULTRA LUBRICATING EYE DROPS — LEADER ULTRA LUBRICATING EYE DROPS (POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1758-2026·2026-04-08

    Burlington Medical BAT coverage may lose radiation attenuation over time

    Burlington Medical is recalling BAT (Breast, Axilla and Thyroid) Coverage because of the potential for attenuation degradation over time.

    Product
    Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1742-2026·2026-04-08

    MiniMed 770G insulin pump delivery varies with pump height changes

    Medtronic is recalling MiniMed 770G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1747-2026·2026-04-08

    MiniMed 620G insulin pump delivery varies with pump height changes

    Medtronic is recalling MiniMed 620G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    MiniMed 620G Insulin Pump (MMT-1750)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1711-2026·2026-04-08

    Medline anterior hip pack contains recalled Olympus biopsy valves

    Medline is recalling the Anterior Hip Pack because it contains recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.

    Product
    MEDLINE ANTERIOR HIP PACK DYNJ64672B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1755-2026·2026-04-08

    Burlington Medical kilts may lose radiation attenuation over time

    Burlington Medical is recalling kilts made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.

    Product
    Burlington Medical, Kilt
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1756-2026·2026-04-08

    Burlington Medical frontal aprons may lose radiation attenuation over time

    Burlington Medical is recalling frontal aprons made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.

    Product
    Burlington Medical, Frontal Aprons
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1708-2026·2026-04-08

    Medline endoscopy kits contain recalled Olympus biopsy valves shedding fragments

    Medline is recalling BAL and ENDO kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.

    Product
    Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1691-2026·2026-04-08

    Medline ENFit G-tube connector kits may leak from dimensional defect

    Medline is recalling kits containing ENFit G-tube connectors because the connectors were not made to required dimensional specifications and may not form a proper seal.

    Product
    Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFITDISCKIT ENFIT DISCHARGE KIT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1680-2026·2026-04-08

    Philips Azurion 5 M20 X-ray may not start from foot switch

    Philips is recalling the Azurion 5 M20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1686-2026·2026-04-08

    Artoura breast tissue expander infusion set needles may be blunt

    Mentor Texas is recalling Artoura Breast Tissue Expanders because the infusion sets may contain a dull or blunt needle tip that may be difficult to advance or may break.

    Product
    Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600cc, 750cc, 850cc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1709-2026·2026-04-08

    Medline laryngoscopy bronchoscopy kits contain Olympus valves shedding rubber fragments

    Medline is recalling four bronchoscopy and laryngoscopy kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.

    Product
    Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY, DYNJ900898I DYNJ901922G 2. FLEXIBLE BRONCHOSCOPY KIT, DYKM1417I DYKM1417J 3. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146A 4. RIGID KIT, DYNDA2138A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1687-2026·2026-04-08

    Artoura ultra high profile expander infusion needles may be blunt

    Mentor is recalling Artoura Breast Tissue Expanders in the smooth ultra high profile range because the infusion sets may contain a dull or blunt needle tip.

    Product
    Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH Smooth Ultra High Profile Tissue Expander, 350cc, 455cc, 535cc, 650cc, 700cc, 850cc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V221000·2026-04-08

    Forest River Recalls 2026 Travel Trailers Due to Incorrect Weight Labeling

    Forest River is recalling 2026 Westbrook and Avenger travel trailers because the Federal Placard label may list an incorrect dry weight, potentially leading to vehicle overloading.

    Product
    FOREST RIVER — FOREST RIVER AVENGER, WESTBROOK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V218000·2026-04-06

    2024 Genesis G90 seat belt anchors may detach in crash

    Hyundai is recalling certain 2023–2026 Genesis G90 vehicles because driver and passenger seat belt anchors may detach. Detached anchors cannot adequately restrain occupants in a crash, increasing injury risk.

    Product
    HYUNDAI — HYUNDAI, GENESIS SANTA FE HYBRID, IONIQ 6, SANTA FE, G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V219000·2026-04-06

    Greenpower Recalls School Buses Due to Missing Mirror Warning Label

    Greenpower is recalling 2020-2024 Nano Beast and 2021-2024 Beast school buses because a warning label on the cross-view mirror may be missing, potentially increasing crash risk.

    Product
    GREENPOWER — GREENPOWER NANO BEAST SCHOOL BUS, BEAST SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V217000·2026-04-06

    Pierce Recalls Firetrucks Due to Faulty Stabilizer Indicator Light

    Pierce Manufacturing is recalling 2015-2026 aerial firetrucks because a faulty light may falsely indicate the vehicle is stable, increasing injury risk during operation.

    Product
    PIERCE — PIERCE IMPEL, ENFORCER, ARROW XT, VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·PHA-04012026-01·2026-04-06

    USDA Retracts Lead Alert for Dorada Chicken Nuggets

    USDA FSIS retracted a public health alert for Dorada chicken nuggets after follow-up testing confirmed the initial lead result was a laboratory error.

    Product
    Dorada Foods — FSIS Retracts Public Health Alert for Frozen, Ready-to-Eat Chicken Nuggets Due to Updated Laboratory Result
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V216000·2026-04-03

    Mercedes-Benz Recalls Vehicles for Drive Shaft Universal Joint Breakage Risk

    Mercedes-Benz is recalling specific 2018-2020 E-Class and S-Class models because the drive shaft universal joint may break, causing a sudden loss of drive power and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S 560 4MATIC COUPE, E 450 4MATIC, E 400 4MATIC, E 400 4MATIC CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26382·2026-04-02

    Universal Broadmoore canopy bed beams can collapse when bed is moved

    Samson International is recalling Universal Broadmoor Bellevue and Oaklynn canopy bed frames because the canopy beams can collapse. Four consumers sustained contusion injuries.

    Product
    Universal Broadmoore brand Bellevue and Oaklynn model canopy bed frames
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26379·2026-04-02

    HTRC and Haisito battery chargers can ignite causing fires

    Huizhou Haitan Technology is recalling T400 battery chargers because they can ignite or cause a connected battery to ignite. Thirty-three fires and explosions have been reported.

    Product
    HTRC and Haisito battery chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide