State

Rhode Island product recalls

73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28801–28825 of 76771

HighFDA (Devices)·Z-2894-2020·2020-09-02
Karl Storz Flexible DCI Intubation Fiberscope Recall for Sterilization Instructions
Karl Storz is recalling 463 Flexible DCI Intubation Fiberscopes to provide updated sterilization instructions. The update prevents the use of specific trays and ethylene oxide sterilization to avoid introducing infectious agents into patient airways.
Product
Flexible DCI Intubation Fiberscope, Part: 11301BND1, with Instruction Manual: Z18445US - Product Usage: are intended to be used for examination and visualization of a patient s upper airway and for aiding placement of an endotracheal tube.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V533000·2020-09-02
Volkswagen Recalls 2020 Passat Vehicles Due to Air Bag Defect
Volkswagen is recalling 2020 Passat vehicles because the passenger air bag may deploy with excessive force, increasing injury risk.
Product
VOLKSWAGEN — VOLKSWAGEN PASSAT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2892-2020·2020-09-02
Karl Storz Flexible Intubation Fiberscopes Recalled for Sterilization Instruction Updates
Karl Storz Endoscopy is recalling 1,246 flexible intubation fiberscopes to provide updated sterilization instructions. The update prevents the use of specific trays and ethylene oxide on certain models to avoid incomplete sterilization.
Product
Flexible Intubation Fiberscope, Part: 11301BN1, with Instruction Manual: Z18441US - Product Usage: are intended to be used for examination and visualization of a patient s upper airway and for aiding placement of an endotracheal tube.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2893-2020·2020-09-02
Karl Storz Flexible Intubation Fiberscope Recall for Sterilization Instructions
Karl Storz is recalling 650 flexible intubation fiberscopes to provide updated sterilization instructions. The update prevents the use of specific trays and ethylene oxide on certain scopes to avoid patient infection.
Product
Flexible Intubation Fiberscope, Part: 11302BD2, with Instruction Manual: Z18445US - Product Usage: are intended to be used for examination and visualization of a patient s upper airway and for aiding placement of an endotracheal tube.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2836-2020·2020-09-02
Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination
Datascope Corporation is recalling Intra-Aortic Balloon Catheters due to potential endotoxin contamination. The recall affects 29,653 kits distributed worldwide.
Product
Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation Plus 7.5 Fr 40cc IAB Kit P/N: 0684-00-0568-01, 0684-00-0568-01U, 0684-00-0568-05, 0684-00-0568-09 - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of Heart…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20176·2020-09-02
Hanamint Recalls Swivel Rockers and Gliders Due to Fall Hazard
Hanamint is recalling about 12,000 swivel rockers and gliders because the chair's post can separate from the base, posing a fall hazard.
Product
Swivel rocker and glider chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·20V530000·2020-09-02
Utilimaster Metris Recall: Incorrect Payload Labeling May Cause Tire Failure
Shyft Group is recalling 2020 Utilimaster Metris vehicles because the payload capacity on the Tire and Loading Information label may be higher than the actual capacity, increasing the risk of tire failure and crashes.
Product
UTILIMASTER — UTILIMASTER METRIS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20E063000·2020-09-02
Ultimate Leather Recalls Zone HS1100 Motorcycle Helmets for Safety Standard Non-Compliance
Ultimate Leather is recalling Zone HS1100 motorcycle helmets manufactured between 2014 and 2016 because they may not adequately protect the wearer in a crash.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2840-2020·2020-09-02
Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination
Datascope Corporation is recalling Intra-Aortic Balloon Catheters due to potential endotoxin contamination. The recall covers kits distributed worldwide.
Product
Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 40cc IAB Kit P/N: 0684-00-0480-01, 0684-00-0480-01U, 0684-00-0480-01C, 0684-00-0480-02, 0684-00-0480-02C, 0684-00-0480-02U, 0684-00-0480-07, 0684-00-0480-08, 0684-00-0480-10
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2835-2020·2020-09-02
Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination
Datascope is recalling 32,855 Intra-Aortic Balloon Catheter kits due to potential endotoxin contamination. The affected products were distributed worldwide.
Product
Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 40cc IAB Kit P/N: 0684-00-0470-01, 0684-00-0470-01U, 0684-00-0470-07, 0684-00-0470-09 - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of Heart Failure.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2878-2020·2020-09-02
Ortho VITROS XT3400 Chemistry System Recalled for Erroneous Results
Ortho Clinical Diagnostics is recalling VITROS XT3400 Chemistry Systems because slides in Slot 18 may be mis-positioned, leading to erroneous test results.
Product
VITROS XT3400 Chemistry System, Product code 6844458
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2841-2020·2020-09-02
Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination
Datascope Corporation is recalling 2,550 kits of Trans-Ray 7Fr 34cc Intra-Aortic Balloon Catheters due to potential endotoxin contamination. The affected devices were distributed worldwide.
Product
Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 34cc IAB (Japan) Kit P/N: 0684-00-0545-01- Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of Heart Failure.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2891-2020·2020-09-02
Karl Storz Flexible Intubation Video Endoscope Recall for Sterilization Instructions
Karl Storz is recalling 2,083 flexible intubation video endoscopes to provide updated sterilization instructions. The update prevents the use of specific trays and ethylene oxide sterilization to avoid introducing infectious agents into patient airways.
Product
Flexible Intubation Video Endoscope, Part: 11301BNX, with Instruction Manual: Z18444US - Product Usage: are intended to be used for examination and visualization of a patient s upper airway and for aiding placement of an endotracheal tube.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2881-2020·2020-09-02
Klarity Vacuum Bags Recalled for Inadequate Vacuum Retention During Radiation Therapy
Klarity Medical Products LLC is recalling 111 vacuum bags used for patient positioning during radiation therapy because they may not hold a vacuum adequately for the required treatment time.
Product
Klarity Vacuum Bags, Item Nos. R7504-30C, R7504-35BC,R7504-35C, R7644-32.5BC, RC7221-25BC, RC7504-17.5C - Product Usage: To be used by trained medical professionals for the stable support and positioning of patients undergoing external beam radiation therapy treatment in a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2906-2020·2020-09-02
Neurovision Cobra x5 EMG Endotracheal Tubes Recalled for Insulation Defect
Neurovision is recalling Cobra x5 EMG endotracheal tubes because the electrode insulation may soften and damage, potentially stopping EMG signal transmission.
Product
Cobra x5 2-Ch EMG ET Tube, 6.0mm, REF: LTE700DCS-5, Rx Only, Sterile EO UDI: B006LTE700DCS52/$$7062618C - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2907-2020·2020-09-02
Neurovision Cobra x5 EMG ET Tube Recalled for Insulation Softening
Neurovision is recalling Cobra x5 2-Ch EMG ET Tubes because the electrode insulating material may soften over time, potentially damaging the device and stopping EMG signal transmission.
Product
Cobra x5 2-Ch EMG ET Tube, 7.0mm, REF: LTE700DCM-5, Rx Only, Sterile EO UDI: B006LTE700DCM52 - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient ventilation…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2845-2020·2020-09-02
Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination
Datascope Corporation is recalling 6,111 Intra-Aortic Balloon Catheter kits due to potential endotoxin contamination. The affected products were distributed worldwide.
Product
Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 30cc IAB (Japan) Kit P/N: 0684-00-0559-01 - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of Heart Failure.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2838-2020·2020-09-02
Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination
Datascope is recalling Intra-Aortic Balloon Catheters due to potential endotoxin contamination. The recall affects 1,746 kits distributed worldwide.
Product
Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 25cc IAB Kit P/N: 0684-00-0478-01, 0684-00-0478-01C, 0684-00-0478-01U 0684-00-0478-02, 0684-00-0478-02U - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2848-2020·2020-09-02
Siemens Cios Alpha and Spin Mobile X-Ray Systems Recalled for Electrical Malfunction
Siemens is recalling Cios Alpha and Cios Spin mobile X-ray systems because a hardware error could cause permanent loss of imaging functionality.
Product
Cios Alpha (VA20) - Model: 10308191 Cios Alpha (VA30) - Model: 11105200 Cios Spin (VA30) - Model: 10308194 Cios Alpha and Cios Spin are a mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2900-2020·2020-09-02
Neurovision Nerveana x5 RLN Monitoring Kit Recalled for Insulation Defect
Neurovision is recalling Nerveana x5 RLN Monitoring Kits because the electrode insulating material may soften, potentially stopping EMG signal transmission and rendering the device unusable.
Product
Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 6.0mm REF NVTKIT-C6-5, Rx Only, Sterile, UDI: B006NVTKITC652/$$7061918A - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2901-2020·2020-09-02
Neurovision Nerveana x5 RLN Monitoring Kit Recalled for Insulation Defect
Neurovision Medical Products Inc. is recalling Nerveana x5 RLN Monitoring Kits because the electrode insulating material may soften, potentially stopping EMG signal transmission and rendering the device unusable.
Product
Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMT ET Tube, 7.0mm REF: NVTKIT-C7-5, RxOnly, Sterile, UDI: B006NvtKITc752/$$7062818C - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2898-2020·2020-09-02
Siemens E.cam and Symbia Systems Recalled for Detector Time Loss
Siemens Medical Solutions is recalling E.cam and Symbia systems with foresight detectors because they may lose detector time information during gated or dynamic acquisitions.
Product
E.cam or Symbia systems that use foresight detectors - Product Usage: To detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588keV.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2904-2020·2020-09-02
Neurovision Cobra EMG ET Tube Recalled for Insulating Material Softening
Neurovision Medical Products Inc. is recalling Cobra x5 1-Ch EMG ET Tubes because the electrode insulating material may soften, potentially damaging the device and stopping signal transmission.
Product
Cobra x5 1-Ch EMG ET Tube, 7.0mm, REF LTE700M-5, Rx Only, Sterile EO CE UDI: B006LTE700M52/$$7061418C - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2899-2020·2020-09-02
RayCare Oncology Software Recalled for Offline Image Review Error
RaySearch Laboratories AB is recalling RayCare oncology software due to an error message that may prevent users from accessing offline images during review tasks.
Product
RayCare, device is stand-alone software - Product Usage: used to support workflows and scheduling, as well as clinical information, planning and treatment management for oncology care.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1539-2020·2020-09-02
Ecolab Recalls Hand Sanitizer Due to Discoloration and Foreign Substance
Ecolab Inc is recalling 305 drums of 55-gallon hand sanitizer nationwide due to discoloration and the presence of a foreign substance.
Product
Hand Sanitizer (Alcohol 80% v/v) topical solution, 55 US GAL (208 L) EcoLab Inc 1 EcoLab Place St. Paul, MN 55102 USA, NDC 47593-624-21
Category
Drug
Distribution
Distributed nationwide