State
73,827 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,054 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 708 (23%) are Severe.
Which agencies issued them
These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
GlaxoSmithKline is recalling Sensodyne Complete Protection toothpaste because wood fragments were found in the product.
Remel Inc is recalling PathoDx Strep B Grouping Latex because a reagent may cause weak reactions, potentially leading to failure to identify target species.
Advanced Sterilization Products is recalling 1,465 STERRAD 100NX wall charts because they contain incorrect instructions regarding instrument tray wrapping.
Merit Medical Systems is voluntarily recalling 950 ReSolve Locking Drainage Catheters because the unit labeling may not match the actual device in the package.
GlaxoSmithKline is recalling Sensodyne Complete Protection toothpaste because wood fragments were found in the product. Consumers should stop using the affected tubes.
GlaxoSmithKline is recalling Biotene toothpaste because wood fragments were found in the product. Consumers should stop using the affected tubes.
Biotronik is recalling specific pacemaker programmer software versions because they are not approved for use in the United States.
GlaxoSmithKline is recalling Biotene PBF toothpaste because wood fragments were found when the product was extruded.
GlaxoSmithKline is recalling 325,504 tubes of Sensodyne toothpaste because wood fragments were found when the product was extruded.
GlaxoSmithKline is recalling Biotene Gentle Mint Gel tubes because wood fragments were found in the product. Consumers should stop using the affected lots.
Stryker is recalling 21 units of a shoulder trial instrument because the package contained the wrong part number.
Abbott Point Of Care Inc. is recalling specific lots of i-Stat PT/INR Cartridges because they may generate excessive star outs, potentially delaying patient results.
Cadence Inc. is recalling 1,665 non-sterile Micro-Mate Tuberculin Glass Syringes because graduation marks are not centered with numeric position marks.
GlaxoSmithKline is recalling Sensodyne toothpaste tubes because wood fragments were found in the product. Consumers should stop using the affected tubes.
GlaxoSmithKline is recalling Biotene fluoride toothpaste because wood fragments were found in the product. Consumers should stop using the affected tubes.
Stryker Howmedica Osteonics is recalling 26 Triathlon tibial inserts because one unit was found in a package labeled for a different catalog number.
Fresenius Kabi USA is recalling 93,000 vials of Hydralazine Hydrochloride Injection because the expiration date printed on the secondary packaging is incorrect.
Forest River is recalling 32 Starcraft transit buses due to an improperly routed cable that may cause an electrical short and fire.
E-One is recalling 2013-2016 Pumpers, Tankers, and Rescue vehicles because the master power switch does not link to the start circuit, allowing operation without lights or sirens.
Rite Aid is recalling about 13,000 outdoor dining sets because chair arms and legs can bend, causing users to fall and potentially be injured.
Mack is recalling 2011-2016 Granite trucks because an air brake reservoir may have insufficient volume, potentially affecting braking performance and increasing crash risk.
IKEA is recalling PATRULL nightlights because the plastic cover can detach, exposing electrical components and posing a shock hazard.
Tvilum is recalling Stars Mix n'Match Chairs sold at Copenhagen Imports because the legs can break, posing a fall hazard.
Turtle Top is recalling certain 2014-2015 transit buses because the back-up camera system may display reversed images, increasing the risk of a crash.
Forest River is recalling 2013-2014 Starcraft All Star XL and 2013 XLT transit buses because fuel injectors may fail, potentially causing engine stalls and increasing crash risk.