The Recall Desk

State

Rhode Island product recalls

73,817 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,054
Critical
221
Severe
708
Most recent
2026-11-04

Of the 3,054 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 708 (23%) are Severe.

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46876–46900 of 76871

  • HighFDA (Devices)·Z-0916-2017·2017-01-04

    GE Healthcare Recalls X-Ray Systems Due to CRT Monitor Fall Risk

    GE Healthcare is recalling specific X-ray systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.

    Product
    SFX
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Devices)·Z-0906-2017·2017-01-04

    GE Healthcare Recalls CRT Monitors Due to Potential Fall Hazard

    GE Healthcare is recalling specific CRT monitors due to the potential for the units to fall. The recall affects multiple system models including ADVANTX and Prestige.

    Product
    ADVANTX LCLP+
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Devices)·Z-0901-2017·2017-01-04

    Medtronic NIM EMG Endotracheal Tubes Recalled for Exposed Wire Hazard

    Medtronic Xomed is recalling NIM EMG Endotracheal Tubes because wire in the tubing can become exposed, posing potential harm to intubated patients.

    Product
    NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17064·2017-01-04

    Toshiba Laptop Battery Packs Recalled for Overheating and Fire Hazards

    Toshiba is expanding a recall of Panasonic lithium-ion battery packs for laptops due to overheating, burn, and fire risks. No injuries have been reported.

    Product
    Panasonic battery packs used in Toshiba laptop computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0909-2017·2017-01-04

    GE Healthcare Recalls Legacy Systems Due to CRT Monitor Fall Risk

    GE Healthcare is recalling Legacy and other imaging systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.

    Product
    Legacy
    Category
    Medical Device
    Distribution
    41 states
  • ModerateFDA (Food)·F-0906-2017·2017-01-04

    Bio-Botanica Recalls Vitamin D-3 Drops for Excess Dosage

    Bio-Botanica is recalling Nature's Answer and Seeking Health Vitamin D-3 drops because the lots contain more Vitamin D3 than the label claims.

    Product
    Liquid VITAMIN D-3 Drops distributed under the following private labels and sizes: a) NATURE'S ANSWER VITAMIN D-3 DROPS DIETARY SUPPLEMENT, 0.5 FLUID OZ/15 mL, UPC 8300026132 -- Nature's Answer Hauppauge, NY 11788; and b) Seeking Health Optimal Vitamin D, Liquid Vitamin D-3…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0240-2017·2017-01-04

    Virtus Pharmaceuticals Recalls Virt-Select Prenatal Softgels Due to GMP Deviations

    Virtus Pharmaceuticals is recalling Virt-Select Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert for cGMP deviations.

    Product
    Virt-Select Prenatal/Postnatal Softgels, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-249-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0903-2017·2017-01-04

    Ortho-Clinical Diagnostics Recalls VITROS Intact PTH Reagent Packs

    Ortho-Clinical Diagnostics is recalling VITROS Intact PTH Reagent Packs due to a positive bias of up to 20% and an incorrectly set reference interval.

    Product
    VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN 10758750006287 / Product Code 6802892 - Reagent Pack, 2) UPN 10758750006250 / Product Code 6802893 - Calibrators For the quantitative measurement of intact parathyroid hormone (iPTH) in human serum and plasma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0241-2017·2017-01-04

    VirtPrex Prenatal Tablets Recalled Due to API Manufacturer Import Alert

    Virtus Pharmaceuticals is recalling VirtPrex Prenatal/Postnatal Tablets because the active ingredient manufacturer is on an FDA Import Alert.

    Product
    VirtPrex Prenatal/Postnatal Tablets, Prescription Supplement Containing Folic Acid and DHA, packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-348-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0235-2017·2017-01-04

    Care-Tech Recalls Surgical Hand Scrub Due to Labeling and Cap Defects

    Care-Tech Laboratories is recalling Techni-Care Surgical Hand Scrub because bottles have missing or illegible lot and expiration dates, as well as defective or cracked caps.

    Product
    Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation (3.0% w/v Chloroxylenol), packaged in a) 4 oz. bottles (NDC 46706-201-01), b) 8 oz bottles (NDC 46706-201-02), c) 16 oz. bottles (NDC 46706-201-03), d) 12 oz. pumpette (NDC 46706-201-05), e) 32 oz. bottles…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0239-2017·2017-01-04

    Virtus Pharmaceuticals Recalls Extra-Virt Plus DHA Prenatal Softgels

    Virtus Pharmaceuticals is recalling 2,406 bottles of Extra-Virt Plus DHA Prenatal/Postnatal Softgels because the API manufacturer is on FDA Import Alert.

    Product
    Extra-Virt Plus DHA Prenatal/Postnatal Softgel, Prescription Multivitamin/Mineral Dietary Supplement with Fish-Based DHA , packaged in 30-count bottle, Rx only, Made in Canada, NDC 76439-251-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0238-2017·2017-01-04

    Virt-Advance Prenatal Softgels Recalled Due to API Manufacturer Import Alert

    Virtus Pharmaceuticals is recalling Virt-Advance Prenatal/Postnatal Softgels because the active ingredient manufacturer is on an FDA Import Alert.

    Product
    Virt-Advance Prenatal/Postnatal Softgels, Prescription Folic Acid Containing Dietary Supplement, packaged in 90-count bottle, Rx only, Made in Canada, NDC 76439-357-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E001000·2017-01-03

    Takata Frontal Passenger Air Bag Inflator Rupture Recall

    Takata is recalling certain frontal passenger air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E002000·2017-01-03

    Takata Frontal Passenger Air Bag Inflator Module Recall

    Takata is recalling specific frontal passenger air bag inflators in 2012 vehicles registered in 14 states and territories due to a risk of rupture.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V002000·2017-01-03

    Audi Recalls 2012-2017 Models for Coolant Pump Fire Risk

    Volkswagen Group of America is recalling specific Audi models because a blocked coolant pump can overheat and cause a fire.

    Product
    AUDI — AUDI A4 ALLROAD, A6, Q5, A5
    Category
    Vehicle
    Distribution
    Distributed nationwide