State
72,940 recalls have nationwide distribution and so reach Rhode Island. 3,043 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,043 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 570 (19%) are Severe.
Which agencies issued them
These figures cover only the 3,043 recalls whose distribution notice names Rhode Island specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays, 12 Fr x 13 cm, over a potential issue with the seal integrity of the header bag packaging.
Integra LifeSciences is recalling 1,198 TruDi Navigation System Multi Instrument Adapters because certain revision combinations may not meet specified accuracy for locating a device in the anatomy.
Total Joint Orthopedics is recalling 103 Klassic BiPolar Heads over a potential packaging issue that could compromise the sterile barrier and present a risk of infection if implanted.
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with curved extensions, 12 Fr x 20 cm, over header bag seal integrity.
Elekta is recalling 338 Leksell Vantage Stereotactic System components because paint flakes from the engravings may separate and could inadvertently enter the wound.
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays, 12 Fr x 16 cm, over a potential issue with the seal integrity of the header bag packaging.
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions and IC components, 12 Fr x 24 cm, over header bag seal integrity.
AquaStar is recalling 3,600 cases of Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp because the shrimp may be contaminated with Cesium-137.
Beckman Coulter is recalling 2,932 units of SYNCHRON Systems Direct LDL Cholesterol reagent from one lot because it may generate false high results.
AquaStar is recalling 9,900 cases of Best Yet Frozen Raw EZ-Peel White Shrimp across multiple counts because the shrimp may be contaminated with Cesium-137.
Aero Healthcare is recalling two lots of AERO TAB caplets because the outer box states acetaminophen and caffeine while the inner pouch correctly states aspirin and caffeine.
AquaStar is recalling 3,600 cases of Waterfront Bistro Frozen Raw EZ-Peel White Shrimp 21/25 because the shrimp may be contaminated with Cesium-137.
Winnebago is recalling 2025-2026 Micro Minnie travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire risk.
AquaStar is recalling 2,916 cases of Publix Large Shrimp Peeled & Deveined Tail On 31/40 because the shrimp may be contaminated with Cesium-137.
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions, 12 Fr x 20 cm, over header bag seal integrity.
AquaStar is recalling 1,800 cases of AquaStar 13/15 Raw Shrimp Easy Peel Deveined, sold at Publix, because the shrimp may be contaminated with Cesium-137.
AquaStar is recalling 5,220 cases of AquaStar Raw Peeled Tail-on Shrimp Skewers because the shrimp may be contaminated with Cesium-137.
B-K Medical is recalling 496 bk3000 ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.
B-K Medical is recalling 1,697 Ultrasound System 1300 bkSpecto units because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.
B-K Medical is recalling 895 bk5000 ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.
B-K Medical is recalling 124 bk3500 ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.
B-K Medical is recalling 567 Ultrasound System 2300 bkActiv units because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.
B-K Medical is recalling 4,426 1202 Flex Focus ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.
Wabash is recalling 2025-2026 Stepdeck trailers because incorrect rear impact guards may have been installed, potentially failing to protect following vehicles in crashes.
Keystone RV Company is recalling 2024-2026 Voltage recreational trailers because incorrectly installed generator fuel lines may cause a fire.