State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
1888653 Ontario Inc. is recalling specific EVOS Full Face Modular Helmets that may not adequately protect the wearer's head in a crash and lack required safety labeling.
Forest River is recalling 2017 Georgetown motorhomes because extra seat belts allow more passengers than the vehicle's weight rating supports, increasing crash risk.
AR500 Armor is recalling Level III body armor that may fail to stop bullets, posing a risk of gunshot injury or death.
Daimler Trucks is recalling specific 2017 Freightliner, Western Star, and FCCC trucks because an engine control module defect may cause the engine to stall without restarting, increasing crash risk.
360 Electrical is recalling three models of surge protectors because they can short circuit when non-grounded plugs are connected, posing a shock or fire hazard.
Rhino Metals is recalling Bighorn P-20 handgun security safes because they can be opened without a combination, posing a serious risk of injury to children and others.
Far East Brokers is recalling about 6,000 children's chairs and swings because the screen-printing contains excessive lead, violating federal standards. No injuries have been reported.
Southeast Toyota Distributors is recalling 2015-2016 Toyota and Scion vehicles because the load carrying capacity label may be incorrect, potentially leading to vehicle overload.
Volkswagen Group of America is recalling 2007-2009 Audi A8 and S8 vehicles because the sunroof glass may not be properly secured and could detach while driving.
Akorn, Inc. is recalling specific lots of Sulfacetamide Sodium Ophthalmic Solution because they failed antimicrobial effectiveness testing, raising concerns about sterility.
Invisiblu International LLC is recalling LGD-Xtreme capsules containing unapproved ligandrol because the product was marketed without an approved NDA or ANDA.
FDA is recalling Curity All Purpose Sponges due to compromised sterility from a barrier breach. The recall affects units distributed in the US and 20 other countries.
Covidien LLC is recalling Vistec X-Ray Detectable Sponges because a breach of the barrier packaging may have compromised sterility.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
Covidien LLC is recalling Curity Gauze Sponges because a breach of the barrier packaging may have compromised their sterility.
Forest River is recalling 2015 Glaval Synergy transit buses because steering boxes may wear prematurely, risking loss of steering control.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.
Newmar is recalling 2014-2016 Dutch Star motorhomes because a defective steering box may cause loss of steering control.
Terex Advance is recalling 338 model year 2016 Front Discharge Concrete Mixer trucks because a weld failure could cause the main chute to detach while driving, increasing crash risk.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility caused by a breach of the barrier.
Pentax Medical is recalling 423 Video Duodenoscopes nationwide after reports of carbapenem-resistant Enterobacteriaceae (CRE) infection at a medical facility.
FDA is recalling Kerlix X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.
The FDA is recalling Kerlix X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.