State
20,188 recalls have nationwide distribution and so reach Rhode Island. 0 additional recalls listed Rhode Island 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 Rhode Island 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.
Daimler Trucks is recalling certain 2022 Freightliner Cascadia trucks because the electronic parking brake may fail to engage when turned off, risking vehicle rollaway. Owners should contact dealers for free repair.
General Motors is recalling certain 2022 Chevrolet Silverado and GMC Sierra trucks with an accessory sport bar. The high-mounted brake light may not function or may be blocked, reducing visibility to other drivers and increasing crash risk.
About 1,160 sling carriers sold on Walmart.com through Joybuy Marketplace Express are recalled due to violations of federal safety standards. The carriers pose suffocation and fall hazards to infants because they lack required structural integrity, occupant retention, and proper restraint systems.
Chrysler is recalling 2022 RAM 2500 and 3500 vehicles due to an ABS control module software malfunction that can disable the electronic stability control system, increasing crash risk. Dealers will provide a free software update.
Spectrum Brands is recalling about 102,000 units of FURminator deShedding Ultra Premium Dog Conditioner (1 Gallon) because the product can contain Pseudomonas aeruginosa bacteria, which poses a serious infection risk to people with weakened immune systems or external medical devices.
GM is recalling 2024-2025 Chevrolet Corvettes because front seat belt retractors may lock and become inaccessible. This prevents seat belts from restraining occupants in a crash, increasing injury risk.
Chrysler recalls 2023 RAM 1500, 2500, and 3500 vehicles with a transmission control unit weld defect that may cause transmission fluid to leak onto electrical components, resulting in loss of drive power or park function.
Gulf States Toyota is recalling 2022-2024 Toyota Highlander L and Highlander LE vehicles with the Blackout Package because their installed tires have insufficient load rating and may fail, increasing crash risk.
Salewa USA recalls Wild Country Ropeman 1 ascenders because the teeth can fail to engage, making it difficult or impossible to ascend. About 7,700 units sold in the United States since December 2022.
Revive Rx Pharmacy recalls 751 vials of compounded tirzepatide (Lot #748127) labeled to contain tirzepatide but actually filled with testosterone cypionate. Patients receiving this medication may take the wrong drug with serious health consequences.
Medline endotracheal tubes with subglottic suctioning may have inflation tubes that detach or tear and suction pumps that disconnect, risking loss of ventilation control.
Imprimis NJOF, LLC is recalling Epinephrine-Lidocaine preservative-free intraocular injection vials (74,440 units) nationwide due to lack of sterility assurance.
Maribel's Sweets 9-piece signature boxes are recalled nationwide due to undeclared coconut. Consumers with coconut allergies should not consume this product.
Ford is recalling certain 2021-2023 Bronco vehicles because first-row seat belt latch plates may be difficult to access, potentially preventing occupants from wearing their seat belts and increasing crash injury risk.
Boston Scientific is recalling Vercise Genus Deep Brain Stimulation devices that may reset during system checks while charging. The reset causes temporary loss of stimulation and may lead to symptom worsening.
Lupin Pharmaceuticals is recalling Cefdinir for Oral Suspension due to defective container seals. The recall affects 51,006 bottles distributed nationwide with lot numbers F305184, F305185, and F305186.
Escape Trailer is recalling 2021-2022 Escape travel trailers (models 17, 19, 21, and 5.0TA) due to cracked quick disconnect fittings in the LP gas system that may cause a gas leak and fire hazard.
Stryker Orthopaedics is recalling Mako surgical robot software due to an error that occurs when switching between surgical applications without restarting the system, resulting in treatment delays.
Stryker Neurovascular is recalling 81 neurovascular devices due to inadequate endotoxin testing. The devices may contain excessive endotoxin levels, which can cause fever, shock, and aseptic meningitis.
Maribel's Sweets is recalling Mother's Day love purse boxes because they contain undeclared coconut, which poses an allergen risk to consumers with coconut allergies.
Dr. Reddy's Laboratories recalls Zoledronic Acid Injection 5mg/100mL due to lack of sterility assurance and leaking vials. Lot #G3000010 with 13,880 vials was distributed nationwide.
Agilent Technologies recalls Dako CoverStainer microscope slide stainers due to potential plexiglass door breakage that could cause injury.
The BD Pyxis MedStation 4000 Auxiliary Tower may allow fluid to enter the system, potentially causing smoke, system downtime, and fire. The FDA Class II recall affects 35,029 units distributed worldwide.
Maribel's Sweets, Inc. is recalling 4,011 boxes of 6-piece signature ganache chocolate boxes due to undeclared coconut. Consumers with coconut allergies are at risk.
Philips Interventional Hemodynamic Application software versions 1.2.0–1.3.1 may not correctly synchronize pressure wave data when acquiring measurements from two devices simultaneously.