State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kawasaki is recalling 2,383 motorcycles because rear shock absorber mount holes can elongate, potentially affecting shock operation and increasing crash risk.
Smiths Medical is recalling CADD Medication Cassette Reservoirs that may have been manufactured with an incorrect pressure plate. The recall covers units distributed worldwide.
Precision Dose Inc. is recalling Carbamazepine Oral Suspension USP unit dose cups because they tested below the required potency specifications.
AvKARE is recalling 274 cartons of Duloxetine Delayed-release Capsules 20 mg due to slightly elevated levels of phthalic acid.
Teva Pharmaceuticals is recalling specific lots of Dutasteride and Tamsulosin HCl capsules because they failed dissolution specifications.
Sanofi-Aventis is recalling 422 vials of Clofarabine injection because the authorized generic product was packaged with the incorrect package insert for the brand name product.
Subaru is recalling 2018 Crosstrek vehicles because an incorrect floor mat retention bracket may allow the mat to interfere with pedals, increasing crash risk.
Norco Bicycles is recalling specific children's models because the cranksets can bend or break during use, posing a fall hazard.
Crysteel is recalling 2017 dump bodies built on Isuzu NRR-Series chassis because the driveshafts may detach from the rear universal joint, potentially causing loss of propulsion and increasing crash risk.
Forest River is recalling 2018 Puma recreational trailers because the federal placards list incorrect tire size and pressure information, which could lead to over-inflation and tire failure.
Triumph is recalling 2016-2017 Speed Triple S and R motorcycles because a charging system wire may rub against a bracket, potentially causing an electrical short and engine stall.
Jayco is recalling 2016-2018 Jay Flight SLX trailers because the battery circuit lacks overcurrent protection, increasing fire risk during electrical shorts.
Phoenix Motorcars is recalling 2015-2017 Zeus 300 and 305 shuttle vans because rear tires may fail when fully loaded, increasing crash risk.
Highland Ridge RV is recalling 2018 Light recreational trailers because the safety chains are rated for a lower weight than the trailer's actual capacity, increasing crash risk if detached.
Entegra is recalling 2016-2018 Aspire, Anthem, Cornerstone, and Insignia motorhomes because they lack required reflectors, reducing visibility to other drivers.
JW Crawford is recalling about 1,300 children's rain ponchos because the hood drawstrings pose a strangulation hazard to kids.
Kidde is recalling fire extinguishers with plastic handles and Pindicator models because they may fail to discharge or have nozzles detach. One death and 16 injuries have been reported.
Van-Con is recalling 2007-2017 Dual Rear Wheel school buses because the seat barrier behind the driver may be pinned, preventing it from deforming in a crash.
REV is recalling 2017-2018 Fleetwood Jamboree and Holiday Rambler Vesta motorhomes because hydraulic lines may not be secured, posing a fire or crash risk.
Thor Motor Coach is recalling 2018 Ace, Axis, Hurricane, Windsport, and Vegas motorhomes because trailer light wiring may be inserted incorrectly, causing lights to fail and increasing crash risk.
Lucky Mart Inc. is recalling Piyamping Anti-Itch Lotion because it contains dexamethasone instead of the labeled hydrocortisone.
Whole Foods Market Brand 365 is recalling 365 Organic Raisin Bran Flakes because peanut butter and cocoa balls were mistakenly packaged in the boxes, creating an undeclared peanut allergen risk.
Vitility is recalling MAN OF STEEL capsules because FDA analysis found they contain undeclared sildenafil, an unapproved drug with unestablished safety and efficacy.
Banner Pharmacy Services is recalling 2,792 syringes of Succinylcholine 200 mg/10 mL because the product lacks assurance of sterility.
Banner Pharmacy Services is recalling ephedrine sulfate syringes because the company cannot ensure the product is sterile.