The Recall Desk

State

Rhode Island product recalls

72,936 recalls have nationwide distribution and so reach Rhode Island. 3,043 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,043
Critical
221
Severe
570
Most recent
2026-09-09

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.

These figures cover only the 3,043 recalls whose distribution notice names Rhode Island specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3101–3125 of 75979

  • HighFDA (Devices)·Z-1401-2026·2026-02-25

    Line insertion kits recalled over sterilization equipment calibration issues

    Medline is recalling 553 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) KIT ACES INSERT PEG, Model Number: DYKMBNDL130; 2) KIT ACES INSERT PEG, Model Number: DYKMBNDL130A; 3) KIT ACES INSERT PERCUTANEOUS T, Model Number: DYKMBNDL4; 4) NICU LINE CHANGE TRAY, Model Number: LC295; 5) OSC SHERMAN KNEE ARTHRO BASIC, M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1406-2026·2026-02-25

    Choice drape packs recalled over sterilization equipment calibration issues

    Medline is recalling 72 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) DRAPE PACK-CHOICE, Model Number: DYNJ63118A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1427-2026·2026-02-25

    Stryker MOLLI 2 System Recall: Marker Dislodgement Risk

    Stryker is recalling the MOLLI 2 System due to magnetized surgical tools that may dislodge markers during target tissue removal procedures. The recall affects 5,864 units distributed worldwide.

    Product
    MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195028 MS-00009 (Pack of 10) - MOLLI Introducer (12cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195134 MP2001 - MOLLI 2 Wand UDI (GTIN): 008500241951
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1367-2026·2026-02-25

    Catheter cutdown trays recalled over damage to the outer tray

    Bard Peripheral Vascular is recalling 14,935 Broviac 4.2 Fr single-lumen CV catheter cutdown trays because damage to the outer tray can potentially compromise the sterile barrier.

    Product
    Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1407-2026·2026-02-25

    Triple lumen insertion kits recalled over sterilization calibration issues

    Medline is recalling 15 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION, Model Number: DYNDM1031A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1426-2026·2026-02-25

    Cervical disc implants recalled after 5mm product was labeled 6mm

    Centinel Spine is recalling 20 Prodisc C SK total cervical disc replacements because products were mislabeled as the 6mm product but included the 5mm product.

    Product
    Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description: Total cervical disc replacement Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1374-2026·2026-02-25

    Olympus Thunderbeat 5 mm 45 cm Front-Actuated Grip Medical Device Recall

    Olympus Corporation of the Americas is removing Olympus Thunderbeat 5 mm, 45 cm Front-Actuated Grip devices due to reports of adverse events.

    Product
    Olympus Thunderbeat, 5 mm, 45 cm Front-Actuated Grip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1389-2026·2026-02-25

    Arteriogram and catheter kits recalled over sterilization calibration issues

    Medline is recalling 30,958 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.

    Product
    Medline Convenience Kits: 1) OR ARTERIOGRAM, Model Number: CDS985094F; 2) KIT SURG ONC LAP DIAG/CV CATH, Model Number: DYKMBNDL153; 3) KIT ACES INSERT PERCUTANEOUS T, Model Number: DYKMBNDL4A; 4) KIT ACES INSERT PERCUTANEOUS T, Model Number: DYKMBNDL4B; 5) VEIN PROCEDURE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V110000·2026-02-25

    2026 Toyota Corolla front headlights missing aim markings

    Toyota is recalling certain 2026 Corolla vehicles due to missing headlight aim markings that can result in improperly aimed headlights, increasing crash risk and glare for oncoming drivers.

    Product
    TOYOTA — TOYOTA COROLLA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V108000·2026-02-24

    Newmar motorhome hood stop adhesive may fail allowing detachment in transit

    Newmar is recalling certain 2018-2026 Bay Star and Bay Star Sport motorhomes because the hood stops mounting adhesive may fail, allowing the hood stop to detach while the vehicle is in transit.

    Product
    NEWMAR — NEWMAR BAY STAR, BAY STAR SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V107000·2026-02-24

    Newmar Recalls 2026 Freedom Aire Motorhomes Due to Wiring Defect

    Newmar is recalling 2026 Freedom Aire motorhomes because a wiring error may cause the heating system to activate unintentionally, producing harmful gas.

    Product
    NEWMAR — NEWMAR FREEDOM AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V109000·2026-02-24

    Thomas Built Buses Recalls 2027 Saf-T-Liner C2 School Buses for Heater Hose Defect

    Daimler Trucks North America is recalling 2027 Thomas Built Buses Saf-T-Liner C2 school buses because a heater hose may rupture, causing hot coolant to leak into the passenger compartment.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V105000·2026-02-23

    Kia Telluride front seat back frames may not restrain occupants

    Kia is recalling certain 2025 Telluride vehicles with power front seats because a manufacturing error may leave the driver and passenger seat back frame assemblies unable to properly restrain occupants in a crash.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V106000·2026-02-23

    Subaru Recalls 2025-2026 Hybrid Vehicles for Fuel Cap Seal Defect

    Subaru is recalling 2025 Forester and 2026 Crosstrek hybrids because a faulty fuel cap seal may cause fuel to spill when the tank is near full and temperatures rise.

    Product
    SUBARU — SUBARU CROSSTREK HYBRID, FORESTER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·006-2026·2026-02-22

    Rosina Recalls Frozen Meatballs Due To Possible Metal Contamination

    Rosina Food Products is recalling approximately 9,462 pounds of frozen Bremer meatballs due to possible metal contamination. The products were distributed to Aldi locations nationwide.

    Product
    Rosina Food Products, Inc. — Rosina Food Products, Inc. Recalls Ready-To-Eat Frozen Meatball Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V098000·2026-02-20

    Demers Ambulances Recall FXP174 Models for Seat Floor Strength Defect

    Braun Industries is recalling 2025-2026 Demers FXP174 ambulances because the floor may not securely hold seats during a crash, increasing injury risk.

    Product
    Demers Ambulances — Demers Ambulances FXP174
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V100000·2026-02-20

    Rossmonster Recalls 2023-2025 Baja Motorhomes Due to Brake Line Routing

    Rossmonster is recalling 2023-2025 Baja Ex and Baja LX motorhomes because incorrectly routed front brake lines may contact tires, causing leaks and reduced braking performance.

    Product
    ROSSMONSTER — ROSSMONSTER BAJA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V103000·2026-02-20

    Volvo EX30 high voltage battery may short circuit and overheat

    Volvo is recalling certain 2025 EX30 vehicles because the high voltage battery may experience a short circuit and overheat. Owners are advised to limit charging to a maximum of 70%.

    Product
    VOLVO — VOLVO EX30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V104000·2026-02-20

    Ford Vehicles Recalled for Integrated Trailer Module Software Defect

    Ford is recalling multiple 2021–2026 trucks, vans, and sport utility vehicles because the integrated trailer module may lose communication with the vehicle when towing, causing loss of trailer brake and turn signal lights or brake function.

    Product
    FORD — FORD, LINCOLN E-TRANSIT, EXPEDITION, F-550 SD, F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V102000·2026-02-20

    Orange EV Recalls T-Series and e-TRIEVER Trucks for Door Lock Defect

    Orange EV is recalling 2018-2026 T-Series and e-TRIEVER trucks because driver's side door handles may lack a lock, potentially failing federal safety standards.

    Product
    ORANGE EV — ORANGE EV T-SERIES ELECTRIC TRUCK, E-TRIEVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V099000·2026-02-20

    Mercedes-Benz eSprinter Recalled for Insufficient Pedestrian Warning Sounds

    Daimler Vans USA is recalling 2025 Mercedes-Benz eSprinter vehicles because they fail to make sufficient pedestrian warning sounds when in reverse, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ESPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2026·2026-02-19

    Ajinomoto Recalls Frozen Chicken Fried Rice Due to Glass Contamination

    Ajinomoto Foods North America is recalling frozen chicken fried rice products due to possible glass contamination. No injuries have been reported.

    Product
    Ajinomoto Foods North America — Ajinomoto Foods North America, Inc. Recalls Chicken Fried Rice Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V097000·2026-02-19

    Range Rover panoramic sunroof side trim may not be properly secured

    Land Rover is recalling certain 2023-2026 Range Rover and Range Rover Sport vehicles because the panoramic sunroof side finisher trim may not be properly secured and can detach.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide