State

Rhode Island product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35251–35275 of 76791

SevereFDA (Devices)·Z-1216-2019·2019-05-15
Alpha Omega Engineering Recalls Neuro Omega Systems Due to Tissue Harm Risk
Alpha Omega Engineering is recalling 29 Neuro Omega Systems because improperly connected cables may cause high charge density, leading to tissue harm.
Product
Neuro Omega System, incorporating HaGuide software. For neurological and neurosurgical use. To monitor, record and display bioelectric signals, and stimulate nerves and brain tissue.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1308-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Seal Defects
Conmed Corporation is recalling specific lots of the Anchor Tissue Retrieval System because seal defects may compromise the product's sterility.
Product
ConMed Anchor Tissue Retrieval System, 8 MM, 125 ML (5/BX) Catalog Number:TRS-ROBO-8 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1295-2019·2019-05-15
Siemens Cios Alpha C-arm X-ray System Recalled for Component Wear
Siemens is recalling two Cios Alpha mobile X-ray systems because continuous high-output operation may cause premature failure of radiation components.
Product
Cios Alpha with software version VA30-mobile C-arm x-ray Material # 11105200 Product Usage: The Cios Alpha is a mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications. Clinical applications may include but…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19120·2019-05-15
Hush Recalls Anesthetic Gels and Sprays for Child-Resistant Packaging Failure
Hush is recalling anesthetic gels, sprays, and foam soaps because the packaging does not meet child-resistant closure requirements, posing a risk of poisoning to young children.
Product
Hush gels, sprays and Hush foam soaps
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1302-2019·2019-05-15
Zimmer Biomet Recalls T7 Driver Cannulated AO Due to Fracture Risk
Zimmer Biomet is recalling 5,885 T7 Driver Cannulated AO units because they may fracture, bend, or shear during use.
Product
T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression Screws and Twist-Off Screws are indicated for fixation of bone fractures, fusion of a joint (arthrodesis) or bone reconstruction (osteotomy) of the mid-foot bones, metatarsal and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1309-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Seal Defects
Conmed Corporation is recalling Anchor Tissue Retrieval Systems due to seal defects that may compromise sterility. The recall affects 7,930 units distributed in the US and 13 other countries.
Product
ConMed Anchor Tissue Retrieval System", 12 MM, 300 ML (5/BX) Catalog Number: TRS-ROBO-12 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1304-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Seal Defects
ConMed is recalling Anchor Tissue Retrieval Systems because voids or partial seals may compromise sterility. The recall covers units distributed worldwide.
Product
ConMed Anchor Tissue Retrieval System 10 MM, 235 ML, (5/BX) Catalog Number: TRS100SB2 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1306-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Sterility Seal Defects
ConMed is recalling Anchor Tissue Retrieval Systems due to seal defects that may compromise sterility. The recall covers 5,034 units distributed worldwide.
Product
ConMed Anchor Tissue Retrieval System, 15 MM, 1850 ML (3/BX) Catalog Number:TRS190SB2 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1303-2019·2019-05-15
Zimmer Biomet Recalls T7 Driver Solid AO Due to Fracture Risk
Zimmer Biomet is recalling 1,924 T7 Driver Solid AO units because they may fracture, bend, or shear during use.
Product
T7 Driver Solid AO (Part Number 110018541) Product Usage: The Biomet Headless Compression Screws and Twist-Off Screws are indicated for fixation of bone fractures, fusion of a joint (arthrodesis) or bone reconstruction (osteotomy) of the mid-foot bones, metatarsal and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1285-2019·2019-05-15
Cardinal Health Recalls ChemoPlus Goggles Due to Latex Mislabeling
Cardinal Health is recalling ChemoPlus Protective Wrap-around Goggles because the kit labels state they are latex-free, but the goggle straps contain natural rubber latex.
Product
ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1286-2019·2019-05-15
Cardinal Health Recalls ChemoPlus Chemo Spill Kits Due to Latex
Cardinal Health 200, LLC is recalling ChemoPlus Chemo Spill Kits because the safety goggles inside contain natural rubber latex, despite the kit label stating the product is latex-free.
Product
ChemoPlus Chemo Spill Kit, Home Health Kit Product Code:DP5108K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19122·2019-05-15
Beaba Recalls Babycook Neo Steam Cookers Due to Glass Bowl Laceration Hazard
Beaba is recalling Babycook Neo steam cooker/blenders because the glass bowl can shatter, posing a laceration hazard. Consumers should stop using the product and contact Beaba for a free replacement.
Product
Babycook Neo steam cooker/blenders
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1305-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Seal Defects
ConMed is recalling Anchor Tissue Retrieval Systems because voids or partial seals may compromise the sterility of the product.
Product
ConMed Anchor Tissue Retrieval System 15 MM, 1550 ML (3/BX) Catalog Number: TRS175SB2 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body cavity during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1307-2019·2019-05-15
ConMed Anchor Tissue Retrieval System Recalled for Seal Defects
Conmed Corporation is recalling the Anchor Tissue Retrieval System due to seal defects that may compromise sterility.
Product
ConMed Anchor Tissue Retrieval System, VATS, 15 MM, 1550 ML (3/BX) Catalog Number: TRS-VATS-15 The Anchor Tissue Retrieval System" by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and removal of an organ or tissue from the body…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1298-2019·2019-05-15
Siemens Cios Alpha Mobile X-ray System Recalled for Component Wear
Siemens is recalling 257 Cios Alpha mobile X-ray systems because continuous high-output use may cause premature failure of radiation components.
Product
Cios Alpha, Model Number 10308191 Mobile X-ray system - Product Usage: The Cios Alpha is a mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications. Clinical applications may include but are not limited to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1283-2019·2019-05-15
Cardinal Health Recalls ChemoPlus Spill Kits Due to Latex Mismatch
Cardinal Health is recalling ChemoPlus chemotherapy spill kits because the safety goggles inside contain natural rubber latex, despite the kit label stating the product is latex-free.
Product
ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1289-2019·2019-05-15
Ortho-Clinical VITROS 3600 Immunoassay System Software Recall
Ortho-Clinical Diagnostics is recalling VITROS 3600 Immunoassay System software versions 3.3.2 and below due to a luminometer malfunction that may prevent the processing of MicroWell assays.
Product
VITROS¿ 3600 Immunoassay System-Software V3.3.2 & below Product Code: 6802783 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1300-2019·2019-05-15
Siemens Atellica IM 1600 Analyzer Recalled for Software Issues
Siemens Healthcare Diagnostics is recalling 366 Atellica IM 1600 Analyzers due to multiple issues identified in the system software that required an update.
Product
Atellica IM 1600 Analyzer, Material Number 11066000
Category
Medical Device
Distribution
36 states
ModerateFDA (Devices)·Z-1288-2019·2019-05-15
Ortho-Clinical VITROS 5600 Systems Recalled for Luminometer Malfunction
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems due to a luminometer malfunction that may prevent the processing of MicroWell assays.
Product
VITROS¿ 5600 Integrated System Refurbished-Software V3.3.2 & below Product Code: 6802915 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1294-2019·2019-05-15
Medica Wash1 Solution Recalled for Ineffective Probe Cleaning
Medica Corporation is recalling Wash1 solution because it fails to clean the probe effectively, potentially causing test interference on the EasyRA analyzer.
Product
Medica Wash1-Wash solution used prior to Lipase assay on the EasyRA clinical chemistry analyzer REF 10680 - Product Usage: For use in washing the probe of the Medica EasyRA Chemistry Analyzer. The wash solution in the wedge is used to prevent interference between certain…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1299-2019·2019-05-15
Siemens Atellica IM 1300 Analyzer Recalled for Software Issues
Siemens Healthcare Diagnostics is recalling 277 Atellica IM 1300 Analyzers due to multiple issues identified in the system software that required an update.
Product
Atellica IM 1300 Analyzer, Material Number 11066001
Category
Medical Device
Distribution
36 states
ModerateFDA (Devices)·Z-1291-2019·2019-05-15
Ortho-Clinical Diagnostics Recalls VITROS XT 7600 Systems Due to Luminometer Malfunction
Ortho-Clinical Diagnostics is recalling 62 VITROS XT 7600 Integrated Systems worldwide because a luminometer malfunction may prevent the processing of MicroWell assays.
Product
VITROS¿ XT 7600 Integrated System-Software V3.4.1 & below Product Code: 6844461 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1284-2019·2019-05-15
Cardinal Health Recalls ChemoPlus Spill Kits Due to Latex Inconsistency
Cardinal Health is recalling ChemoPlus chemotherapy spill kits because the safety goggles inside contain natural rubber latex, despite the kit label stating the product is latex-free.
Product
ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1293-2019·2019-05-15
Ortho-Clinical VITROS ECi Immunodiagnostic System Recalled for Luminometer Malfunction
Ortho-Clinical Diagnostics is recalling 25 refurbished VITROS ECi Immunodiagnostic Systems because a luminometer malfunction may prevent the processing of MicroWell assays.
Product
VITROS ECi Immunodiagnostic System Refurbished Product Code: 6801059 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1297-2019·2019-05-15
Elekta Unity Systems Recalled for Missing Contrast Agent Warnings
Elekta Limited is recalling nine Elekta Unity systems because the user manual lacks a warning regarding the administration of unvalidated contrast agents.
Product
Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance Imaging is indicated for radiation therapy treatments and stereotactic radiation treatments of malignant and benign diseases anywhere in the body as determined by a licensed medical practitioner in…
Category
Medical Device
Distribution
Distributed nationwide