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.
MobilityWorks is recalling 667 Ford E-series vans equipped with specific Ricon wheelchair lifts. Defective pivot holes may allow bearings to shift, causing the lift platform to fall and injure the operator.
Kermit, Inc. is recalling 16 oz bottles of Hot & Spicy Key Lime Barbecue Sauce due to undeclared soy on the label.
Kermit, Inc. is recalling 455 bottles of Key Lime Ginger Wasabi Marinade because the label fails to list soy and wheat ingredients.
JD & SN Inc. is recalling 13 vials of 80 mg testosterone pellets because the FDA cannot ensure the sterile compounded drugs are free from contamination.
Kermit, Inc. is recalling 12-ounce bottles of Key Lime Cocktail Sauce due to undeclared soy on the label.
Encore Medical is recalling 277 Turon Shoulder Impaction Fixtures because polymer material wore off during assembly, potentially contaminating the implant.
Kermit, Inc. is recalling Kermit's P4 Hot Sauce because the product label fails to declare soy, a major food allergen.
Kermit, Inc. is recalling 16 oz bottles of Key Lime Barbecue Sauce due to undeclared soy on the label.
Abbott Laboratories is recalling 65 ARCHITECT i2000SR diagnostic systems worldwide because they contain incorrect tubing.
Encore Medical is recalling 634 units of Reverse Shoulder Prosthesis Stem Impaction Fixtures because polymer wear from the fixtures can damage the titanium coating on humeral stems during assembly.
Synthes (USA) Products LLC is recalling 25 units of Threaded Plate Holders that are incorrectly etched with the wrong part number and may not fit into a Small Fragment Plate.
Philips Medical Systems is recalling 109 Ingenuity Core 128 CT systems due to X-ray measurement errors causing image artifacts.
Sentinel CH SpA is recalling 765 kits of Sentinel MULTIGENT Ammonia Ultra Reagent because results may be below the linear range for samples collected in heparin tubes.
Philips Medical Systems is recalling 108 Brilliance 64 CT systems worldwide due to an X-ray measurement error that causes Ring/Dot artifacts.
Philips is recalling 36 Ingenuity Core CT systems worldwide due to an X-ray measurement error that causes Ring/Dot artifacts in images.
Philips Medical Systems is recalling 323 Brilliance 16-Slice CT systems worldwide due to X-ray measurement errors causing Ring/Dot artifacts.
Varian Medical Systems is recalling ARIA Radiation Oncology software versions 10, 11, 13.0, and 13.5 because admin instructions may fail to print or transmit.
Philips Medical Systems is recalling 67 Ingenuity Flex CT systems worldwide due to an X-ray measurement error that causes Ring/Dot artifacts in images.
Encore Medical is recalling 209 Exprt Precision System Revision Knee implants because the labeling is missing size and diameter information.
Becton, Dickinson and Company is recalling two lots of BD CD3 (SK7) FITC in vitro diagnostic reagents due to an error in the Spanish small text on the label.
Prevost is recalling 2016 H3-45 and X3-45 VIP coaches because front suspension studs may fail, allowing a wheel to turn unexpectedly and increasing crash risk.
Newmar is recalling 60 recreational vehicles due to a potential ABS modulator valve fracture that could impair braking performance.
GE is recalling about 33,500 Zoneline air conditioning and heating units due to a risk of fire caused by moisture accumulation and electrical arcing.
Toyota is recalling 2013-2015 Avalon and Lexus ES vehicles because the Pre-Collision System may unexpectedly brake when detecting steel road objects.
Forest River is recalling 217 model year 2016 recreational vehicles because an incorrect shift cable bracket allows the vehicle to be shifted out of park without applying the brakes.