State
73,737 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,053 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 707 (23%) are Severe.
Which agencies issued them
These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Conversio Health is recalling Albuterol 2.5mg / Ipratropium 0.75mg vials nationwide due to a lack of processing controls.
Temple Turmeric Inc. is voluntarily recalling Temple Pure Prana Matcha+Shot bottles due to high levels of yeast. The recall affects 18,732 units distributed to several states.
Washington Homeopathic Products, Inc. is recalling Ferrum Phosphoricum 6X Tablets because they were not manufactured under current good manufacturing practices.
Conversio Health is recalling Albuterol, Ipratropium, and Triamcinolone inhalation vials due to a lack of processing controls.
Washington Homeopathic Products, Inc. is recalling Natrum Muriaticum 6X Tablets because they were not manufactured under current good manufacturing practices.
Conversio Health is recalling Albuterol and Ipratropium inhalation vials nationwide due to a lack of processing controls.
Washington Homeopathic Products, Inc. is recalling 295 bottles of Kali Sulphuricum 6X Tablets because they were not manufactured under current good manufacturing practices.
Washington Homeopathic Products, Inc. is recalling R2103 homeopathic product because it was not manufactured under current good manufacturing practices.
Washington Homeopathic Products, Inc. is recalling 417 bottles of Kali Phosphoricum 6X Tablets because they were not manufactured under current good manufacturing practices.
Conversio Health is recalling Albuterol, Ipratropium, and Budesonide inhalation vials due to a lack of processing controls.
Neocis Inc. is recalling three units of the Neocis Guidance System Fiducial Array because they may mismatch measurement files, resulting in a failed landmark check.
Angiodynamics Inc. is recalling BIOFLO 8F Single Titanium Non-Filled Valved ports because snap lock connectors may not meet specifications, preventing catheter insertion and delaying implantation.
Washington Homeopathic Products, Inc. is recalling Kali Muriaticum 6X Tablets because they were not manufactured under current good manufacturing practices.
X-Gen Pharmaceuticals is recalling Levetiracetam Injection vials because the incorrect package insert version was attached to the product.
T.J. Maxx, Marshalls, and HomeGoods sold about 1,200 units of 19 previously recalled products, including infant sleepers and speakers. Consumers should stop using these items and contact the manufacturers for remedies.
Volvo is recalling 2011-2017 S60 and V60 models because a door latch component may break, potentially allowing doors to open while driving.
BMW is recalling 1999-2001 3-Series vehicles because a replacement driver air bag inflator may absorb moisture, potentially causing it to rupture or underinflate during a crash.
BMW is recalling 1999-2000 323i, 328i, 323Ci, and 328Ci vehicles because driver air bag inflators may rupture or underinflate in a crash, increasing injury risk.
Mark Feldstein & Associates is recalling Stacked Gourd Jack-O-Lantern decorations because the internal wiring can overheat and ignite. Four reports of smoking or fire have been received.
BMW is recalling 1999 323i and 328i vehicles because driver air bag inflators may rupture or underinflate in a crash, increasing injury risk.
Takata is recalling specific non-azide driver air bag inflators used in 1995-2000 vehicles. The inflators may absorb moisture, risking rupture or underinflation during a crash.
Forest River is recalling 2020 XLR Boost trailers because an undersized axle and tire combination may cause the trailer to be overloaded, increasing the risk of a crash.
Yamaha is recalling 2018 and 2019 EF2000iS portable generators because the fuel tank can leak gasoline, posing fire and burn hazards.
The Toro Company is recalling 2017-2019 LC922 towable log splitters because tow bolts may fail, causing the unit to detach or tip over.
Forest River is recalling 2018-2020 Cascade and Cherokee travel trailers because the trailer hitch coupler may fail, potentially causing the trailer to detach from the tow vehicle.