State
72,820 recalls have nationwide distribution and so reach Maine. 3,894 additional recalls listed Maine specifically in their distribution scope.
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.
Target is recalling about 211,000 Cat & Jack Children's Sandals because decorative pearls can fall off and pose a choking hazard to children. No injuries have been reported.
Huish Outdoors recalls Hollis 200LX second stage diving regulators because the inlet tube can crack and break, posing a risk of serious injury or death from drowning. About 7,200 units are affected.
Chrysler is recalling certain 2026 Jeep Gladiator and Wrangler vehicles because the steel wheels may be too thin and crack or detach, risking loss of vehicle control.
TOMY International is recalling approximately 116,908 Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools due to a tip-over hazard that poses a risk of serious injury and death. The company has received 11 reports of the towers being unstable, shifting, or leaning, though no injuries have been reported to date.
Warren James is recalling the copper cup found in Space King No Girls Allowed Relic Lunch Boxes due to high lead concentration levels that pose a lead poisoning hazard. Consumers should stop using the recalled cups immediately.
Jaguar Land Rover North America, LLC is recalling certain 2021-2025 Land Rover Discovery vehicles because insufficient drain holes may cause rearview camera damage, reducing driver visibility.
Panasonic is recalling about 11,480 Model NB-G200 Electric Toaster Ovens because the power cord insulation may be insufficient, posing a shock and fire risk. No fires or injuries have been reported, but four consumers reported tripped circuit breakers.
Bortezomib for Injection 3.5mg/Vial manufactured by Reliance Life Sciences is being recalled nationwide due to lack of sterility assurance. Affected lots include RBIH0125A, RBIH0225A, RBIH0325A, and RBIH0525A distributed across the USA.
Elekta, Inc. is recalling Advanced Gynecological Applicators due to potential detachment of the intrauterine tube tip, which may remain inside a patient during cancer treatment.
Elekta is recalling the Geneva Brachytherapy Applicator due to a safety concern that the tip of the intrauterine tube may detach and remain inside a patient during cancer treatment.
Think Surgical is recalling TMINI Femur and Tibia Tracking Arrays used in knee replacement surgery because the knob on the tracking array may loosen, causing potential misalignment of the array.
Reliance Life Sciences is recalling Azacitidine for Injection 100mg/Vial nationwide due to lack of sterility assurance. Patients using affected lots should contact their healthcare provider.
Somerset Therapeutics is recalling Pemetrexed for Injection 100mg/Vial due to lack of sterility assurance. The recall affects approximately 12,000 vials distributed nationwide.
Elekta's Fletcher CT/MR Shielded Applicator Set is recalled due to risk that the tip of the intrauterine tube may detach and remain inside a patient during gynecological brachytherapy treatment.
E-One is recalling 2025-2026 Cyclone N, Typhoon N, and Commercial emergency vehicles because the drive/pump mode transfer case may disengage, causing loss of rear-wheel power.
Reliance Life Sciences is recalling Pemetrexed for Injection 500mg/Vial nationwide due to lack of sterility assurance. The affected product may not meet required sterility standards for intravenous use.
Orange EV is recalling 2020-2026 electric trucks because improper welding may cause frame rails to crack and separate, increasing the risk of loss of control.
High Valley Orchard Chocolate Covered Raisins (15oz bags) are recalled nationwide due to undeclared peanut from mis-packaging. Consumers with peanut allergies should not consume this product.
Siemens is recalling an A1c blood test assay (Material Number 11097536) for the Atellica CH and Atellica CI analyzers due to potential intermittent bias that could cause falsely high or low hemoglobin A1c patient results.
Boston Scientific is recalling Intracept Access Instruments due to potential sterile barrier breach in the outer tray seal, which could introduce infection risk.
WALLAC OY is recalling GSP Neonatal GALT Kit units due to reduced on-board stability that may increase run-QC failures and delay patient test results.
Gasco Industrial Corp. is recalling Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% (32 oz.) due to subpotency. Affected lots 250206B1, 250218B2, and 250507B1 were distributed nationwide in the US.
Olympus Corporation of the Americas is replacing the previous design of its Single Use Distal Cover (MAJ-2315) with a newly designed version for use with EVIS EXERA III Duodenovideoscopes.
Nissan is recalling certain 2020–2026 Nissan Armada and 2011–2027 Infiniti QX56/QX80 vehicles with 22" wheels because the Gross Axle Weight Rating on the certification label is incorrect, which can allow the vehicle to be overloaded and increase crash risk.
ConvaTec is recalling Aquacel Ag Surgical SP dressings (Lot 5G00809) that were manufactured with greater-than-specified thickness. The dressing is used in surgical wound care.