State
73,096 recalls have nationwide distribution and so reach Maryland. 8,223 additional recalls listed Maryland specifically in their distribution scope.
Of the 8,223 recalls naming Maryland we have scored against our rubric, 996 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,134 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,223 recalls whose distribution notice names Maryland specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Motiv Power Systems is recalling 2017-2023 F-59 school buses because a missing heat shrink insulator and retention clip may cause 12-volt control wires to deteriorate, leading to a loss of drive power and increased crash risk.
General Motors is recalling 2013-2019 Chevrolet Express and GMC Savana Cutaway vans because brake lines may rub against body mounts, causing leaks and potential brake failure.
Newmemo Children's Ring Sets sold on Amazon contain unsafe levels of lead and cadmium. These toxic metals can cause adverse health effects if ingested by young children.
Caframo Limited is recalling about 2,140 model 9421 cabinet heaters sold in the U.S. because a crimp holding a wire in place is not properly finished and can detach, creating an electrocution hazard.
Polaris is recalling certain Model Year 2023–2024 Sportsman 850, XP 1000, and XP 1000 S ATVs because fuel can leak at the fuel pump outlet, creating a fire hazard. The company has received 14 reports of fuel leaks and 3 reports of fire, with no injuries reported.
Polaris is recalling Model Year 2024 RANGER XD 1500 and Crew XD 1500 recreational off-road vehicles equipped with winches because the winch wiring can overheat during use, creating a fire hazard and risk of serious injury.
About 137,000 Lucid platform beds with upholstered square tufted headboards can sag, break, or collapse during use. The manufacturer has received 245 reports of structural failure resulting in 18 reported injuries.
Motiv Power Systems is recalling specific 2017-2023 electric chassis vehicles because a missing wiring harness component may cause a loss of drive power, increasing crash risk.
Jo-Ann Stores recalls about 9,700 Place & Time battery-operated desk lamps due to fire hazard from overheating battery compartments during USB charging. No injuries reported, but three incidents of battery melting or popping have been documented.
GM is recalling certain 2023-2024 Chevrolet Colorado and 2023 GMC Canyon vehicles because a front seat belt buckle attachment bolt may not have been tightened properly.
Wee Gallery is recalling about 8,000 Baby Tummy Time Gallery products because the clear plastic pockets contain phthalate levels that exceed federal limits. Phthalates are toxic if ingested by young children.
Olympus Corporation recalls 4,507 Triangle Tip Electrosurgical Knives (Model KD-640L) due to device fragmentation during use. The issue is linked to reports of serious injury and improper adherence to usage instructions.
Medline Industries is recalling 19 units of semi-rigid suction liners due to reported adverse events involving potential loss of suction during use.
Medline is recalling specific lots of semi-rigid suction liners due to reported adverse events involving potential loss of suction during use.
Olympus Corporation recalled 2,525 electrosurgical knives (KD-645L) nationwide after reports of serious injury from knives breaking off during use. Users must follow Instructions for Use regarding proper electrosurgical unit compatibility and output settings.
Ultradent Products is recalling Transcend Singles Universal Body dental composite resin due to red particulates found during manufacturing. The recall affects approximately 2,450 units distributed in the US and several foreign countries.
Ultradent Products recalls Transcend Econo Kit dental composite due to red particulates in the material from a manufacturing issue. Affected lot C1464 was distributed to dental professionals in 34 U.S. states and internationally.
Zimmer GmbH is recalling Biolox Option Taper Sleeves due to mislabeling where packaging labels one neck size but contains the opposite size. These components are used in hip replacement surgery.
Medline Industries recalls specific lots of semi-rigid suction liners in C-section convenience kits due to reported adverse events. The liners may lose suction during intermittent use.
Siemens Healthcare is recalling ADVIA Chemistry urinary protein test reagents due to potential quality control issues that could produce inaccurate patient results.
Sol-Millennium Medical Inc. is recalling multiple syringe models found to differ substantially from their FDA-cleared designs. The recalled products include SOL-M, SOL-CARE, MEDLINE, MONOJECT, and HENRY SCHEIN branded syringes distributed in the United States and internationally.
Medtronic Perfusion Systems is recalling 290 units of DLP Single Stage Venous Cannulae due to a manufacturing error where straight-tip cannulae were placed into packaging labeled for right-angle metal-tip cannulae.
Medline Industries is recalling 1,646 units of semi-rigid suction liners used in surgical kits due to reported adverse events involving potential loss of suction or low suction during intermittent use.
Medline Industries is recalling 134 units of semi-rigid suction liners due to potential loss of suction during intermittent use. The affected kits were distributed worldwide including the US, Canada, and Panama.
Siemens Healthcare Diagnostics is recalling one lot of Dimension Vista Total Bilirubin Flex Reagent Cartridges due to underfilled wells during manufacturing. The defect may result in inaccurate test results for calibrators, quality control, and patient samples.