The Recall Desk

State

Rhode Island product recalls

73,827 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.

Which agencies issued them

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54776–54800 of 76881

  • SevereFDA (Devices)·Z-2326-2015·2015-08-12

    Aesculap S4C Occiput Torque Wrench Recalled Due to Reassembly Defect

    Aesculap is recalling 10 S4C Occiput Torque Wrenches because improper reassembly after reprocessing caused a screw to break during implantation.

    Product
    S4C Occiput Torque Wrench F/Set Screw; used to tighten the S4 Cervical Spinal System clamping screws with a defined torque 2.8 Nm for tightening the clamping screw in the screw head/hook head/occipital plate/transverse connector and other connectors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2317-2015·2015-08-12

    Cook Inc. Recalls Beacon Tip Torcon NB Advantage Catheters

    Cook Inc. is recalling Beacon Tip Torcon NB Advantage Catheters due to reports of tip splits or separation, which may cause loss of function or complications.

    Product
    Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2324-2015·2015-08-12

    Medtronic Passive Biopsy Needle Kit Recalled for Adhesive Defect

    Medtronic is recalling 1,415 Passive Biopsy Needle Kits because compromised adhesive may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.

    Product
    Medtronic Passive Biopsy Needle Kit, Part Number 9733068 - Passive Biopsy Needle Kit. The image guided Passive Biopsy Needle is an accessory instrument with the StealthStation System. The Biopsy Needle is intended to be used for stereotaxy biopsy of brain tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2264-2015·2015-08-12

    Medtronic Recalls EnVeo R Loading Systems Due to Particulate Presence

    Medtronic is recalling EnVeo R Loading Systems because of the presence of particulate. The recall affects 6,912 units worldwide, including 540 in the US.

    Product
    EnVeo R Loading System, Model No. LS-EnVeoR-23, LS-EnVeoR-2629, LS-EnVeoR-23-C, LS-EnVeoR-2629-C. Cardiovascular valve delivery system for use with the Medtronic CoreValve Evolut R system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V508000·2015-08-12

    Jeep Renegade Recall for Radio Software Vulnerability

    Chrysler is recalling 2015 Jeep Renegade vehicles to fix a radio software vulnerability that could allow unauthorized remote control of vehicle systems.

    Product
    JEEP — JEEP RENEGADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2342-2015·2015-08-12

    Siemens Axiom Artis Angiography Systems Recalled for Liquid Seepage Risk

    Siemens Medical Solutions is recalling Axiom Artis angiography systems because liquid may seep through the top cover and penetrate internal components, potentially disabling table movements.

    Product
    Axiom Artis systems, dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V511000·2015-08-12

    Pierce Velocity and Quantum Vehicles Recalled for Headlight Flickering

    Pierce is recalling 2014-2015 Velocity and Quantum vehicles because LED headlamps may flicker in extreme cold, reducing visibility and increasing crash risk.

    Product
    PIERCE — PIERCE VELOCITY, QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2344-2015·2015-08-12

    Siemens ACUSON S Family Ultrasound Systems Recalled for Biopsy Guide Defect

    Siemens is recalling ACUSON S Family ultrasound systems because biopsy needles may move outside the on-screen guidelines when using specific attachments.

    Product
    ACUSON S Family ultrasound systems utilizing the 18L6 HD and/or 6C1 HD biopsy guidelines 6C1HD - model numbers: 10442008 6C1HD Needle Guide, S3000; 10440586 6C1 HD Biopsy Guide, S2000 18L6 - model numbers: 10442007 18L6 Biopsy Guide, S3000 10044200 S2000 Biopsy Starter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2340-2015·2015-08-12

    Siemens Artis zee Systems Recalled for Potential Liquid Seepage

    Siemens Medical Solutions is recalling Artis zee angiography systems because liquid may seep through the table cover, potentially preventing table movement.

    Product
    Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V507000·2015-08-12

    Nissan Recalls Versa and Versa Note for Pedal Interference Risk

    Nissan is recalling 2012-2015 Versa and 2014-2015 Versa Note vehicles because a center console trim panel may catch the driver's shoe, delaying brake application and increasing crash risk.

    Product
    NISSAN — NISSAN VERSA, VERSA NOTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1283-2015·2015-08-12

    Teva Recalls Amphetamine Tablets Due to Unknown Impurity

    Teva Pharmaceuticals is recalling specific lots of amphetamine tablets because they failed impurity specifications. The product contains an unknown impurity.

    Product
    DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2347-2015·2015-08-12

    Merge Hemo System Recalled for Freeze-Up During Cardiac Procedures

    Merge Healthcare is recalling 451 Merge Hemo systems used with Masimo PHASEIN modules due to system freeze-ups that required moving patients to other cath labs.

    Product
    Merge Hemo, 9.10, 9.20.0, 9.20.1,9.20.2, 9.30, 9.40.0, 9.40.1, 9.40.2 with Massimo PHASEIN End Tidal CO2 (EtCO2) module. Merge Hemo (formerly named HeartSuite Hemodynamics) monitors, measures, and records physiologic data from a human patient undergoing a cardiac…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V509000·2015-08-12

    Chrysler Recalls 2014 Jeep Cherokee for Windshield Wiper Defect

    Chrysler is recalling 2014 Jeep Cherokee vehicles because using front wipers on dry glass may damage the body control module, potentially causing wiper failure and impaired vision.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2932-215·2015-08-12

    Nabisco Fig Newtons Recalled for Undeclared Milk Allergen

    Mondelez International is recalling Nabisco Fig Newtons because the outer carton fails to declare milk, a major allergen, while the inner packaging does.

    Product
    Outer carton : Nabisco Newtons Fig 24-2 OZ (56 g) Packs Net Wt 3 lbs Mondelez International Mondelez Global LLC East Hanover, NJ 07936 USA Made in Mexico case UPC 0 44000 03445 0 Inner Pouch: Nabisco Newtons Fig Net Wt 2 oz (56 g) Mondelez Global LLC, East Hanover, NJ…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V510000·2015-08-12

    Winnebago Recalls 2014-2015 Motorhomes Due to Stuck Deadbolt Locks

    Winnebago is recalling 2014-2015 Itasca and Winnebago motorhomes because deadbolt locks may become stuck, potentially trapping occupants inside the vehicle.

    Product
    ITASCA — ITASCA, WINNEBAGO SPIRIT, VISTA, BRAVE, MINNIE WINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2328-2015·2015-08-12

    Philips HeartStart XL+ Defibrillator Recalled for Software and Hardware Issues

    Philips is recalling 13,168 HeartStart XL+ defibrillators worldwide due to software and hardware issues that can affect device function.

    Product
    Philips HeartStart XL+ Defibrillator/Monitor Product Usage: The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1991-2015·2015-08-12

    Olympus Analytical X-ray Systems Recalled for Higher Scatter Readings

    Olympus Scientific Solutions Americas is recalling 1,047 Analytical X-ray Systems because scatter readings around the probe head were higher than published specifications for certain samples.

    Product
    Olympus Scientific Solutions Americas Analytical X-ray System. Delta, Delta Element, Delta Plus, DPO-4000-XX-U-EN-EN-PM-SP12, DPO-6000-XX-U-EN-EN-AP-SP10. Mobile X-ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2942-2015·2015-08-12

    MedOp Recalls MaxiFlex Multinutrient Formula Due to Out-of-Specification Raw Material

    MedOp Health, Inc. is recalling MaxiFlex Multinutrient Formula dietary supplements because a material review found the Chondroitin Sulfate raw material used was out of specification.

    Product
    ***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***Dietary Supplement ***120 Vegetable Capsules***Distributed by MedOp, Inc., Oldsmar, FL 34677***www.medop.com***.
    Category
    Food
    Distribution
    22 states
  • ModerateFDA (Devices)·Z-2349-2015·2015-08-12

    Zimmer Surgical Recalls Tourniquet Cuffs with Missing Instructions

    Zimmer Surgical Inc. is recalling 330 units of 30-inch tourniquet cuffs because the instructions for use were missing usage instructions and warnings.

    Product
    30inch Dual Port/Single Bladder Disposable Tourniquet Cuff with PLC, Zimmer Surgical, Inc. Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the arterial blood flow in a limb to produce a bloodless operating field. Single bladder…
    Category
    Medical Device
    Distribution
    45 states
  • ModerateFDA (Devices)·Z-2341-2015·2015-08-12

    Siemens Artis Q Systems Recalled for Potential Liquid Ingress

    Siemens Medical Solutions is recalling Artis Q angiography systems because liquid may seep through the top cover, potentially disabling table movements. No injuries have been reported.

    Product
    Artis Q systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2339-2015·2015-08-12

    GE Healthcare Recalls MRI Scanners Due to Potential Image Orientation Errors

    GE Healthcare is recalling 82 MRI scanners because a missing spacer may cause images to be flipped left-right with incorrect orientation annotations.

    Product
    GE Healthcare, Signa Infinity MR System; Signa MR/i MR System; SmartSpeed; EchoSpeed Plus; HighSpeed Plus, Signa Infinity MR System with EXCITE Technology, Excite II, Signa 3T Infinity with Excite, Signa Excite 1.5T and Signa Excite 3T, Signa Excite HD, Signa HD 1.5T and Signa…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1286-2015·2015-08-12

    Perrigo Recalls Subpotent Mometasone Furoate Ointment Tubes Nationwide

    Perrigo Israel Pharmaceuticals is voluntarily recalling 158,268 tubes of Mometasone Furoate Ointment USP, 0.1%, because the product is subpotent.

    Product
    Mometasone Furoate Ointment USP, 0.1%, 15 g tubes, Rx Only, Manufactured by Perrigo, Yeruham 80500, Israel, Distributed by Perrigo, Allegan, MI 49010, NDC 45802-0119-37
    Category
    Drug
    Distribution
    Distributed nationwide