State
73,106 recalls have nationwide distribution and so reach Rhode Island. 3,046 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,046 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 572 (19%) are Severe.
Which agencies issued them
These figures cover only the 3,046 recalls whose distribution notice names Rhode Island specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jayco is recalling 2023-2025 Entegra Aspire motorhomes because an upside-down camera module may overheat, preventing image display and increasing crash risk.
The FDA is recalling FUL-GLO Fluorescein Sodium Sterile Ophthalmic Strips (4,648 cartons) nationwide due to unspecified impurities in the active ingredient exceeding USP standards.
The Biomet OrthoPak Bone Growth Stimulator System is being recalled due to potential lead wire sheath damage that could prevent therapeutic signal delivery and delay patient treatment nationwide.
Howmedica Osteonics is recalling TRIDENTII PSL CLUSTER58F hip replacement acetabular shells due to excessive deburring. The manufacturing defect affects units distributed nationwide and internationally.
EBI, LLC recalls 829 replacement lead wire assemblies (Part 1067724-2) distributed nationwide since May 1, 2023. Damaged wire sheaths may prevent therapeutic treatment signals from reaching electrodes, potentially delaying treatment.
Electro Medical Systems is recalling water bottles used with AIRFLOW dental devices because certain bottle collars can disassemble under pressure during treatment or storage. No injuries have been reported.
Howmedica Osteonics is recalling TRIDENTII HEMI CLUSTER50D hip implant shells due to excessive deburring that may create a smooth edge, potentially affecting implant fit. Affected units were distributed nationwide and internationally.
Baxter Healthcare is recalling Seprafilm Adhesion Barrier units (165 units, Lot DBYSEP046) that were distributed nationwide without FDA approval. Affected units distributed in LA, GA, IN, VA, FL, NY, and CA.
Certain lots of Abilify (aripiprazole) 10 mg tablets are being recalled due to cross-contamination with other products. Affected products were distributed nationwide.
ABILIFY (aripiprazole) 15 mg tablets from lot AMS00223A are being recalled due to cross contamination with other products. The recall affects packages distributed nationwide.
Otsuka America Pharmaceutical is recalling certain lots of Abilify (aripiprazole) 5 mg tablets distributed nationwide due to cross contamination with other products. This is classified as a Class III recall.
Honeywell Inc. is recalling FENDALL 2000 PURE FLOW eyewash solution due to Current Good Manufacturing Practice deviations. The recall affects 10,605 cartridges distributed nationwide in the USA and Canada with expiration dates through June 2025.
Nomax Inc recalls FUL-GLO Fluorescein Sodium Ophthalmic Strips (Lot 14776) nationwide due to API manufacturing specification failures. The active ingredient was not manufactured to current USP standards regarding unspecified impurities.
Abilify (aripiprazole) 30mg tablets are being recalled due to cross-contamination with other products. The affected lots were distributed nationwide in the United States.
Select lots of 3M Durapore Surgical Tape (Catalog Number 1538-118) were labeled with a 5-year shelf life when the actual shelf life is 3 years. The recall affects over 3.5 million rolls distributed worldwide.
Bendix is recalling Intellipark Park Valve Modules where a rubber seal may fracture, causing park brake failure or unexpected engagement.
Braun Ambulances is recalling 29 vehicles from 2023-2024 because a firmware defect can cause electrical circuits to overheat, increasing the risk of fire.
Stellantis is recalling 2021 Alfa Romeo Giulia vehicles because a fuel line sensor housing may crack and leak fuel, increasing the risk of engine stall or fire.
BMW is recalling certain 2020-2024 MINI Hardtop 2 Door (Cooper SE) vehicles because the high voltage battery housing may not have been sealed properly, allowing water to enter the battery.
Nissan is recalling certain 2024 Sentra vehicles because the front left driveshaft may not be fully seated in the CVT assembly, or may have a loose or missing retaining clip.
Starcraft RV is recalling 2023 GSL fifth wheel trailers because the cooktop LED backlight circuit board may overheat, increasing the risk of a fire.
Newmar is recalling certain 2022 Bay Star motorhomes because the LED backlight circuit board in the cooktop range may fail and overheat.
Highland Ridge RV is recalling 681 model year 2022-2023 trailers because an LED backlight circuit board may overheat, increasing the risk of a fire.
Alliance RV is recalling 2024 Avenue travel trailers because an improperly wired inverter circuit could cause a breaker to overheat and increase fire risk.
Reading Truck Body LLC is recalling 2022-2024 RM-78 crane bodies because taillights may be mounted too high, reducing visibility and increasing crash risk.