State
20,187 recalls have nationwide distribution and so reach Maryland. 0 additional recalls listed Maryland specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Maryland consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
GM is recalling 338 2024 Chevrolet Silverado EV vehicles due to an incorrect second-row center seat belt bezel that may damage or tear the seat belt in a crash, potentially failing to restrain occupants.
Forest River Bus is recalling certain 2021 Berkshire coaches due to a faulty retractable awning that may extend unintentionally while the vehicle is in transit. The unintended extension could distract the driver or become a road hazard, increasing the risk of a crash.
Lowe's has recalled about 27,400 Origin 21 oval and rectangle black framed wall mirrors because they can detach from their metal hanging plates and fall, creating laceration and impact hazards. The company has received 15 reports of separation with no injuries yet reported.
RH Baby & Child is recalling about 480 Jeune French Contemporary Upholstered Panel Cribs because cylindrical metal inserts in the wooden frame can become loose and detach, posing a choking hazard to infants.
Papablic Archie Infant Swings (model PAPABLIC61A) pose a suffocation risk because they are designed for infant sleep with an incline angle greater than 10 degrees, violating federal safety regulations. Consumers should stop using them immediately.
Peace Industry Group is recalling about 1,000 Peace Sports Youth All-Terrain Vehicles due to violations of federal ATV safety standards. The ATVs have defective handlebars, faulty parking brakes, missing reflectors, and footguards that pose risks of laceration, amputation, and collision.
Forest River is recalling Coachmen Galleria motorhomes (2020–2024) because battery boost wiring may become damaged, causing an electrical short circuit that results in loss of power steering, increasing crash risk.
Brompton T-Line Foldable Bicycles are recalled because loose steerer clamp bolts can cause misalignment between the handlebar and front wheel, risking loss of steering control and falls. About 1,080 units are affected.
About 55,480 Avocado Organic Cotton Mattress Pad Protectors are being recalled because they violate the federal flammability regulation for mattress pads, posing a fire hazard. No injuries have been reported.
ECHO Inc. is recalling about 3,900 gas-powered backpack blowers due to a fuel supply line that can leak gas, creating a fire hazard. No injuries have been reported.
Attom Tech is recalling about 4,100 LED light-up jelly ring toys sold on Amazon because the button cell batteries inside can be easily accessed and swallowed by children, posing a risk of serious internal injury and death.
Beberoadlove is recalling about 1,940 New Moon Travel Bassinets because they lack a required stand and can fall from elevated surfaces, violating federal safety regulations for infant sleep products. No injuries have been reported.
Medtronic Xomed is recalling NIM Vital Nerve Monitoring systems because they may fail to detect nerve damage or dysfunction. Approximately 7,804 units were distributed worldwide.
B Braun Medical's Perfusor Space Syringe Pump may not properly recognize Cardinal Health Monoject syringes due to manufacturing changes, risking medication overdose, underdose, or therapy delays.
Abbott is recalling 1198 Infinity 7 Implantable Pulse Generators due to potentially incorrect service life indicators and end-of-service dates in product labeling, which could result in loss of therapy.
Zydus Pharmaceuticals (USA) Inc. is recalling Venlafaxine Hydrochloride Extended-Release Capsules USP 37.5mg due to failed dissolution specifications in lots M213175 and M213176. The recall affects 13,128 and 252 bottles distributed nationwide.
LINK BIO CORP is recalling the LINK SymphoKnee Patella Sizing Template (Item Number 881-509/00, Lot C225066) because markings on two arms of the instrument were mixed up during manufacturing.
B Braun's Perfusor Space infusion pump may be incompatible with Cardinal Health Monoject syringes affected by manufacturing changes, creating risks of overdose, underdose, and delayed therapy.
A software issue in certain Siemens Sensis Vibe diagnostic systems may cause the application to crash when documentation features are used during clinical reporting events.
Beckman Coulter has recalled 13,565 units of IGM clinical reagent due to incorrect lipemia check settings that may produce false low results or report high results as normal. Affected units were distributed worldwide.
Siemens Sensis Vibe diagnostic systems may crash when using documentation features during once-per-study event reporting. Three systems are affected; no injuries reported.
Embecta Corp. is recalling BD Nano 2nd Gen Pen Needles that were distributed at or after their February 29, 2024 expiration date. Using expired needles cannot guarantee sterility and integrity.
Medtronic recalled A610 Clinician Programmer software and pocket adaptors (Models 64001, 64002) due to MRI safety restrictions. Patients with these implants are limited to head-only MRI procedures.
Abbott is recalling 5,900 Infinity 5 implantable pulse generators because the replacement indicator and end-of-service date may be shorter than labeled, potentially causing premature device failure. Patients should contact their doctor about device status.
B Braun is recalling Perfusor Space infusion pump kits because Cardinal Health Monoject syringes have manufacturing changes that make them incompatible, potentially causing overdose, underdose, or delayed therapy.