The Recall Desk

State

Rhode Island product recalls

73,576 recalls have nationwide distribution and so reach Rhode Island. 3,048 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,048
Critical
221
Severe
707
Most recent
2026-10-21

Of the 3,048 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 707 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,048 recalls whose distribution notice names Rhode Island specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25376–25400 of 76624

  • HighFDA (Devices)·Z-1889-2021·2021-06-23

    Medtronic perfusion system tubing packs recalled due to weld defects

    Medtronic is recalling specific lots of CB7J98R7 Custom Pack perfusion system tubing because some units may have insufficient or incomplete welds. The defect could affect device performance during cardiac surgery.

    Product
    Medtronic CB7J98R7, Custom Pack CB7J98R7, Custom Pack CB7J98R7 3/8 Pack, Custom Perfusion System, Sterile, Rx.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1881-2021·2021-06-23

    Medtronic Cardiac Perfusion Tubing Packs Recalled Due to Defective Welds

    Medtronic is recalling specific lots of CB4W67R20 Custom Perfusion System tubing packs due to incomplete welds that could affect system performance. The recall affects 61 packs distributed across nine states.

    Product
    Medtronic CB4W67R20, Custom Pack CB4W67R20 Adult E, Custom Perfusion System, Sterile, Rx.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1882-2021·2021-06-23

    Medtronic Perfusion System Tubing Packs Recalled for Weld Defects

    Medtronic is recalling perfusion system tubing packs due to manufacturing defects involving incomplete or insufficient welds. No injuries have been reported, but the defect may affect product performance and safety.

    Product
    Medtronic CB10W64R1, Custom Pack CB10W64R1 CH Access 3/8, Custom Perfusion System, Sterile, Rx.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1884-2021·2021-06-23

    Medtronic Custom Perfusion System Recalled for Incomplete Welds

    Specific lots of Medtronic's CB10W65R1 perfusion system tubing packs may have incomplete or insufficient welds that could compromise system integrity during cardiac surgery.

    Product
    Medtronic CB10W65R1, Custom Pack CB10W65R1 CH Access1/4, Custom Perfusion System, Sterile, Rx.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0629-2021·2021-06-23

    Dr. Reddy's Atorvastatin Calcium Tablets Recalled for Failed Impurity Specifications

    Dr. Reddy's Laboratories is recalling Atorvastatin Calcium Tablets USP 10 mg nationwide because certain lots contain impurities that exceeded acceptable specifications.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1865-2021·2021-06-23

    ACUVUE VITA soft contact lenses recalled for potentially incomplete packaging seals

    Johnson & Johnson Vision Care is recalling certain ACUVUE VITA soft contact lenses due to potential incomplete packaging seals. Only a limited number of packages from LOT # BOOWWWL are affected.

    Product
    ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21E055000·2021-06-22

    Cummins Recalls ISL Remanufactured Diesel Engines Due to Fuel Rail Leak Risk

    Cummins is recalling certain ISL remanufactured diesel engines because a sealing washer may not seat correctly, allowing the high-pressure fuel rail to leak and increasing fire risk.

    Product
    FUEL SYSTEM, DIESEL:FUEL INJECTION SYSTEM:FUEL RAIL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V464000·2021-06-18

    Altec Recalls 2020-2021 Aerial Devices Due to Weak Bolts

    Altec is recalling 2020-2021 AT200A, AT235, and AT235P aerial devices because insufficient strength bolts may fail, causing the pedestal to separate and increasing the risk of injury or death.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V463000·2021-06-18

    Trailstar Recalls 2017-2019 Dump Trailers Due to Steering Arm Defect

    Trailstar is recalling 2017-2019 Dump Trailers because the steering arm may detach, potentially causing loss of steering control or road hazards.

    Product
    TRAILSTAR — TRAILSTAR DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V461000·2021-06-17

    2020-2021 Nissan Sentra Vehicles Recalled for Bent Tie Rod Defects

    Nissan is recalling 2020-2021 Sentra vehicles because the left or right tie rod may be bent. A bent tie rod can break, causing loss of steering control and increasing crash risk.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V462000·2021-06-17

    Thomas Built Buses Recalls School Buses for Seat Protection Defect

    Daimler Trucks North America is recalling 2018-2022 Thomas Built Saf-T-Liner HDX school buses because incorrect seat configurations may fail to provide proper crash protection.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V457000·2021-06-17

    2020-2021 Land Rover Discovery Loose Battery Ground Contact Defect

    Certain 2020-2021 Land Rover Discovery vehicles have a loose battery ground contact causing electrical failure and potential vehicle shutdown while driving. Dealers will replace the ground stud at no cost.

    Product
    LAND ROVER — LAND ROVER DISCOVERY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V455000·2021-06-17

    2021 Chevrolet Tahoe and related GM vehicles power steering software defect

    General Motors recalls certain 2021 Chevrolet Tahoe and related vehicles due to a power steering software issue that may cause loss of steering assist, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, GMC SUBURBAN, ESCALADE ESV, ESCALADE NA, TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V459000·2021-06-17

    Spartan Fire Recalls 2019-2021 S-180 Pumper Emergency Vehicles

    Spartan Fire is recalling 2019-2021 S-180 Pumper emergency vehicles because a pump shift harness defect may prevent the vehicle from shifting into pump mode.

    Product
    SPARTAN FIRE — SPARTAN FIRE S-180 PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V453000·2021-06-17

    2021 Heartland Mallard trailers recalled for potentially leaky LP gas cooktop lines

    Heartland Recreational Vehicles is recalling certain 2021 Mallard and other trailers because LP gas lines on outside cooktops may not have been tightened properly, creating a risk of gas leaks and fire.

    Product
    HEARTLAND — HEARTLAND TRAIL RUNNER, WILDERNESS, NORTH TRAIL, MALLARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V456000·2021-06-17

    Terex Advance Recalls 2021 Front Discharge Mixers Due to Chute Defect

    Terex Advance is recalling 188 units of 2021 Front Discharge Mixers because a shaft key was not installed properly, which could cause unintentional chute movement and increase the risk of injury.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1786-2021·2021-06-16

    Medical Convenience Kits Recalled Due to Mold Contamination Risk

    Avid Medical is recalling 160 fistula care kits due to potential contamination from Aspergillus penicillioides fungal growth in a component applicator. The contamination could breach the kit's package integrity and affect other sterile components.

    Product
    FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit, Avid Medical Part Number: VAMK024-03
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1834-2021·2021-06-16

    Surgical procedure pack anesthetic mislabeled with wrong drug and strength

    DeRoyal Angio Cath Removal Tray contains mislabeled anesthetic; the label indicates 1% Lidocaine but the tray actually contains 0.5% Bupivacaine. This FDA Class I recall affects 60 trays distributed in MS, VA, LA, and NY.

    Product
    DeRoyal Angio Cath Removal Tray, REF 89-9936.02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0747-2021·2021-06-16

    365 Everyday Value Whey Protein Powder Mislabeled with Soy Protein

    365 Everyday Value Whey Protein Powder was mistakenly packaged with Soy Protein Powder. The affected canisters were distributed nationwide and may pose a risk to consumers with soy allergies.

    Product
    365 Everyday Value Whey Protein Powder Natural Vanilla Flavor, Net Wt. 13.9 oz. canisters, UPC 9948228764, Whole Foods Market 550 Bowie Street Austin, TX 78703. Store in a cool, dry place.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1798-2021·2021-06-16

    Jelco Insulin Syringe Graduation Markings Recalled for Skew Defect

    Smiths Medical recalls 1,432,200 Jelco insulin syringes with skewed graduation markings that could lead to incorrect dosing. Specific lot numbers are affected.

    Product
    JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G X 1/2" (0.33mm x 13mm), REF 4428-1 b) 1.0mL 29G X 1/2" (0.33mm x 13mm), REF 4429-1
    Category
    Medical Device
    Distribution
    Distributed nationwide