The Recall Desk

State

Rhode Island product recalls

73,722 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,053
Critical
221
Severe
707
Most recent
2026-10-28

Of the 3,053 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 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31251–31275 of 76775

  • HighFDA (Devices)·Z-1110-2020·2020-02-19

    Terumo Advanced Perfusion Assembly Pump Guts Recalled for Potential Shaft Failure

    Terumo is recalling 16 Advanced Perfusion Assembly Pump Guts units because the pump shafts may fail, potentially causing the pump to stop during surgery.

    Product
    Terumo Advanced Perfusion Assembly Pump Guts, 6 Inch, Catalog Number 801798 - is indicated for use for up to 6 hours in the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1123-2020·2020-02-19

    Flowonix US Clinical 20mL Programmable Pump Recall for Firmware Alarm Defect

    Flowonix Medical Inc is recalling US Clinical 20mL Programmable Pumps because a firmware anomaly may prevent the device from sending error codes or audible alarms during valve system issues.

    Product
    US Clinical 20mL Programmable Pump. Catalog No. 01827 The device is an implantable infusion pump. GTIN-14 00810335020082
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1125-2020·2020-02-19

    Flowonix Prometra II Pump Recall for Firmware Alarm Anomaly

    Flowonix Medical Inc is recalling Prometra II implantable infusion pumps because a firmware anomaly may prevent the device from sending error codes or audible alarms.

    Product
    Prometra II Programmable 20mL Pump. Catalog No. 93827 The device is an implantable infusion pump. GTIN-14 00810335020YYY (YYY= in-country language specific)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0841-2020·2020-02-19

    Pfizer Recalls Caduet Tablets Due to Defective Bottle Seals

    Pfizer is recalling 141 bottles of Caduet tablets because defective bottle rims may have allowed moisture to enter, potentially compromising the medication.

    Product
    CADUET — CADUET (AMLODIPINE AND ATORVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1146-2020·2020-02-19

    Revanesse Versa Recalled for Incorrect Expiration Date Labeling

    Prollenium Medical Technologies is recalling 48,457 kits of Revanesse Versa because the product is labeled with an 18-month expiration date, but it is only approved for 12 months.

    Product
    Revanesse Versa, PN40081
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0842-2020·2020-02-19

    Pfizer Recalls Caduet Tablets Due to Defective Bottle Seals

    Pfizer is recalling 128 bottles of Caduet (amlodipine and atorvastatin) because defective bottle rims may have caused inadequate foil sealing, potentially compromising moisture protection.

    Product
    CADUET — CADUET (AMLODIPINE AND ATORVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0855-2020·2020-02-19

    Lupin Recalls Memantine Hydrochloride Capsules for Dissolution Failure

    Lupin Pharmaceuticals is recalling 6,294 bottles of Memantine Hydrochloride Extended Release Capsules because they failed to meet dissolution specifications during stability testing.

    Product
    MEMANTINE HYDROCHLORIDE — MEMANTINE HYDROCHLORIDE (MEMANTINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1219-2020·2020-02-19

    Bard Intra-abdominal Pressure Monitoring Device Recalled for Potential Leaks

    C.R. Bard Inc. is recalling 1,300 units of the Bard Intra-abdominal Pressure Monitoring Device due to leaks or disconnects that may cause inaccurate readings.

    Product
    The Bard Intra-abdominal Pressure Monitoring Device is composed of a tubing set used for infusing fluid into the urinary bladder through the Foley catheter sampling port. It utilizes a clamping device to occlude the urinary drainage tubing to form a fluid column through which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1228-2020·2020-02-19

    CooperVision Vertex Toric Contact Lenses Recalled for Incorrect Power

    CooperVision is recalling specific lots of Vertex Toric contact lenses because they were manufactured with an incorrect power.

    Product
    Coopervision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 Soft (hydrophilic) Contact Lens (extended wear)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0996-2020·2020-02-19

    Theraflu Cough Relief Recalled for Missing Sodium Warning

    GSK is recalling Theraflu Cough Relief packets because the label lacks a warning for people on sodium-restricted diets.

    Product
    Theraflu Cough Relief, Dextromethorphan HBr and Guaifensin, 6 packets per carton. Distributed by: GSK Consumer Healthcare, Warren, NJ 07059. NDC carton: 0067-6089-01, NDC packet: 0067-6089-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1227-2020·2020-02-19

    CooperVision Vertex Toric Contact Lenses Recalled for Incorrect Power

    CooperVision is recalling 216 units of Vertex Toric contact lenses because they have an incorrect power than expected.

    Product
    Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (extended wear)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0843-2020·2020-02-19

    Par Pharmaceutical Recalls Frovatriptan Tablets Due to Incorrect Expiration Date

    Par Pharmaceutical is recalling 9,936 cartons of Frovatriptan Succinate Tablets, 2.5mg, because they are labeled with an incorrect expiration date.

    Product
    Frovatriptan Succinate Tablets, 2.5mg, packaged in 1 blister card of 9 tablets per carton, Rx Only, Manufactured by: Almac Pharma Services Limited, Craigavon, BT63 5UA, UK; Manufactured for: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 0603-3718-34.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V091000·2020-02-17

    Jayco Recalls Fifth Wheel Trailers Due to Underrated Axles

    Jayco is recalling 2013-2015 Fifth Wheel Seismic and 2015 Pinnacle trailers because they were built with 6,000lb axles instead of the intended 7,000lb axles.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO SEISMIC, PINNACLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V090000·2020-02-14

    Mercedes-Benz Recalls G 550 and AMG G63 for Stability Control Defect

    Mercedes-Benz is recalling 2019-2020 G 550 and AMG G63 vehicles because a faulty electrical resistor may deactivate Electronic Stability Program and Anti-lock Brake System.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 550, AMG G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V088000·2020-02-14

    Kia Recalls Sedona and Sorento Models for ABS Module Fire Risk

    Kia is recalling 2006-2010 Sedona and 2007-2009 Sorento vehicles because moisture in the ABS module can cause an electrical short and engine compartment fire.

    Product
    KIA — KIA SEDONA, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V089000·2020-02-14

    Mercedes-Benz Recalls Vehicles for Instrument Cluster Software Defect

    Mercedes-Benz is recalling specific 2020-2021 models because instrument cluster software may deactivate interior switch illumination, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450, CLA 250, GLS450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V080000·2020-02-13

    RAM Recalls 2019 1500 Trucks for Transfer Case Defect

    Chrysler is recalling 2019 Ram 1500 4WD trucks because a transfer case gear may be installed incorrectly, potentially causing a sudden loss of power or loss of the Park function.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V085000·2020-02-13

    Vermeer Recalls Brush Chipper Trailers Due to Lug Nut Defect

    Vermeer is recalling certain 2016-2020 brush chipper trailers because incorrect lug nuts may loosen, potentially causing the wheel to detach or loss of control.

    Product
    VERMEER — VERMEER AX19, BC1500, BC1000XL, BC1200XL
    Category
    Vehicle
    Distribution
    Distributed nationwide