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.

30551–30575 of 76775

  • ModerateFDA (Devices)·Z-1627-2020·2020-04-08

    Conformis Recalls iTotal CR Knee Replacement System Due to Labeling Error

    Conformis, Inc. is recalling four iTotal CR Knee Replacement System kits because they were labeled with incorrect serial numbers and delivered to the wrong customers.

    Product
    iTotal CR Knee Replacement System, Model No. TCR-121-1111-010102, (ITOTAL CR IPOLY XE IMPLANT KIT LEFT) - Product Usage: The iTotal CR Knee Replacement System is intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1623-2020·2020-04-08

    Gentell Hydrogel Ag Gauze Recalled for FDA Registration Failure

    Gentell, Inc. is recalling 53,134 units of Gentell Hydrogel Ag 2x2 gauze because the product was not properly registered with the FDA.

    Product
    Gentell Hydrogel Ag 2x2, model no GEN-11220 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1617-2020·2020-04-08

    Haemonetics Recalls TEG Manager Software Due to Alert Display Defect

    Haemonetics is recalling TEG Manager software versions 1.1.0 through 4.1.1 because a defect causes incorrect out-of-range alerts for coagulation test results.

    Product
    TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0, 3.0.0, 4.0.0, 4.1.0 and 4.1.1. Intended: For in vitro coagulation studies
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1601-2020·2020-04-08

    Butterfly iQ Ultrasound System Recalled for Lack of FDA Approval

    Butterfly Network, Inc. is recalling 11,183 Butterfly iQ Ultrasound Systems because they were distributed without an approved 510(k).

    Product
    Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction) Tool REF/Model: 850-20003 UDI: (01)00866646000206 Software versions 1.10.0, 1.11.0, 1.12.0, 1.13.0, 1.13.0, 1.14.0, 1.15.0 Product Usage: Intended use: Diagnostic ultrasound imaging and measurement of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1079-2020·2020-04-08

    Lupin Recalls Lisinopril Tablets Due to Foreign Tablet Mix-Up

    Lupin Pharmaceuticals is recalling 25,944 bottles of Lisinopril 30 mg tablets because a 5 mg tablet was found mixed into a 30 mg bottle.

    Product
    LISINOPRIL — LISINOPRIL (LISINOPRIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1628-2020·2020-04-08

    Conformis Recalls iTotal PS Knee Replacement System Due to Labeling Error

    Conformis is recalling two iTotal PS Knee Replacement System kits because tibial trays were labeled with incorrect serial numbers and delivered to the wrong customers.

    Product
    iTotal PS Knee Replacement System, Model No. TPS-111-1111-010101, (ITOTAL PS IPOLY IMPLANT KIT LEFT) Product Usage: The iTotal CR Knee Replacement System is intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1624-2020·2020-04-08

    Gentell Hydrogel Ag Gauze Recalled for FDA Registration Deficiency

    Gentell, Inc. is recalling 20,025 units of Gentell Hydrogel Ag 4x4 gauze because the product was not properly registered with the FDA.

    Product
    Gentell Hydrogel Ag 4x4, model no. GEN-11420 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1600-2020·2020-04-08

    Butterfly iQ Ultrasound System Auto Bladder Volume Tool Recalled for Regulatory Violation

    Butterfly Network, Inc. is recalling the Butterfly iQ Ultrasound System Auto Bladder Volume Tool because it was distributed without an approved 510(k).

    Product
    Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder Volume Tool is a segmentation measurement tool REF/Model: 850-20003 Software versions 1.13.0, 1.14.0, and 1.15.0 - Product Usage: Butterfly iQ is indicated for use by qualified and trained healthcare…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1258-2020·2020-04-08

    Akorn Recalls Fentanyl Citrate Injection Due to Impurity Specification Failure

    Akorn Inc. is recalling Fentanyl Citrate Injection, USP, 100 mcg/2 mL, because retained sample testing showed total impurities exceeded the allowed limit.

    Product
    Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 10 Ampules per carton, (2 mL each), Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-030-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1625-2020·2020-04-08

    Gentell Hydrogel Ag Saturated Gauze Recalled for FDA Registration Deficiency

    Gentell, Inc. is recalling 6,433 units of Gentell Hydrogel Ag Saturated Gauze because the product was not properly registered with the FDA.

    Product
    Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1626-2020·2020-04-08

    Gentell Hydrogel Ag Wound Dressing Recalled for Registration Issues

    Gentell, Inc. is recalling Gentell Hydrogel Ag wound dressings because the product was not properly registered with the FDA.

    Product
    Gentell Hydrogel Ag 4oz. Tube, model no. - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Silver Antimicrobial Wound Dressing is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V201000·2020-04-07

    Vac-Tron Recalls Vacuum Excavator Trailers for Lighting Defects

    Vac-Tron is recalling 2012-2020 vacuum excavator trailers because improper lighting and missing reflectors may reduce visibility at night, increasing crash risk.

    Product
    VAC-TRON — VAC-TRON MC 535, MC 533 SDT, MINICOMBO, MC 573 SDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V204000·2020-04-07

    Vac-Tron Recalls 2012-2020 Vacuum Excavator Trailers for Lighting Defects

    Vac-Tron is recalling 2012-2020 vacuum excavator trailers because improper exterior lighting and missing reflectors may reduce visibility at night, increasing crash risk.

    Product
    VAC-TRON — VAC-TRON MC 873 SDT, MC 855 SDT, MC 833 SDT, MC 835 SDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V198000·2020-04-06

    KTM Recalls 2019-2020 790 Adventure Models Due to Rear Brake Hose Overheating

    KTM is recalling 2019-2020 790 Adventure and 790 Adventure R motorcycles because the rear brake hose may overheat, potentially causing brake failure and increasing crash risk.

    Product
    KTM — KTM 790 ADVENTURE R, 790 ADVENTURE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V193000·2020-04-03

    Isuzu Recalls 2019 NPR Vehicles Due to Brake Line Clip Defect

    Isuzu is recalling 2019 NPR and Chevrolet 4500 vehicles because incorrectly installed brake line clips may cause rear driver-side brake failure.

    Product
    ISUZU — ISUZU NPR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V196000·2020-04-03

    Trans Tech Bus Recalls 2020 Models for Seatbelt Warning Light Defect

    Trans Tech Bus is recalling 446 specific 2020 Roadstar, SST, and ST Aero buses because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition.

    Product
    TRANS TECH — TRANS TECH ROADSTAR, SST, ST AERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V190000·2020-04-02

    Setra S417TC Coaches Recalled for Front Door Detachment Risk

    Daimler Coaches is recalling 2017-2020 Setra S417TC coaches because the front entrance door support frame may be the wrong size, allowing the door to detach while moving.

    Product
    SETRA — SETRA S417 TC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20102·2020-04-02

    Manhattan Toy Recalls Musical Lili Llama Due to Choking Hazard

    Manhattan Toy is recalling Musical Lili Llama wooden activity toys because loose screws can fall off, posing a choking hazard to young children.

    Product
    Musical Lili Llama
    Category
    Consumer Product
    Distribution
    Distributed nationwide