State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Akorn, Inc. is recalling Erythromycin Pledgets USP, 2%, 60-count jars because the active pharmaceutical ingredient failed USP microbial tests.
Full Tilt Ice Cream is recalling Mudhoney ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.
Stryker is recalling MEDPOR BARRIER Sheets due to risks of deformation, cracking, and loss of adhesion during surgery.
Freeland Foods is recalling Go Raw 100% Organic Sunflower Seeds because CFIA detected Salmonella in the product.
Full Tilt Ice Cream is recalling Strawberry Basil ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.
AnazaoHealth Corporation is recalling 51 vials of Compounded Plaquex intravenous injection nationwide because the product contains an active pharmaceutical ingredient from an unapproved source.
La Flor Products Co., Inc. is recalling ground comino in 2 oz, 6 oz, and 5 lb packages due to undeclared peanut protein.
Stryker is recalling MEDPOR BARRIER Sheets due to potential implant deformation, mechanical instability, and cracking during surgery.
Jaguar is recalling 2013 XF vehicles because the fuel pump may shut down, causing the vehicle to stall and lose power-assisted braking and steering.
Virtual Imaging, Inc. is recalling 316 digital mobile X-ray systems in the US and 6 in Canada due to a potential for unintended and erratic motion.
Teleflex Medical is recalling Aquapak 340 SW humidifier adaptors because the packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Siemens Medical Solutions is recalling Symbia T series imaging systems because a linear bearing car may fail, allowing ball bearings to fall out.
Teleflex Medical is recalling Aquapak 340 Humidifier Adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Teleflex Medical is recalling Aqua 540 Humidifier Adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Integra LifeSciences is recalling 1,053 Mayfield Ultra 360 Base Units because the locking handle mechanism may fail during use, posing a risk to patients.
Siemens Medical Solutions is recalling 719 Symbia S series systems because a linear bearing car may fail, allowing ball bearings to fall out.
Teleflex Medical is recalling 040 Humidifier Adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Gillig LLC is recalling 177 S26 Eaton-brand hydraulic pumps sold between 2011 and 2014. The pumps may have manufacturing inconsistencies causing unexpected steering effort changes.
Teleflex Medical is recalling Aquapak sterile water humidifier adaptors because packages may contain black particles.
Medical Components, Inc dba MedComp is recalling 243 hemodialysis catheters and PICCs because a duplicate sterilization process may have rendered included drug products ineffective.
Arthrosurface, Inc. is recalling 143 Taper Post Fixation Components because they were not cleared for marketing in the US with current indications.
Teleflex Medical is recalling Aquapak 640 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Teleflex Medical is recalling Aquapak sterile water humidifier adaptors because packages may contain black foreign particles.
Teleflex Medical is recalling AQUAPAK 640 SW humidifier adaptors because packages may contain black particles. The recall covers 15,779,607 units distributed worldwide.
Gillig LLC is recalling S5510 series wheelchair lifts manufactured by Ricon Corporation between November 2010 and February 2011. The platform side plates may crack, posing a risk of injury if the platform falls.