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.

54901–54925 of 76881

HighFDA (Devices)·Z-2108-2015·2015-07-29
FDA Recalls Devon Light Gloves for Sterility Compromising Defects
The FDA is recalling specific lots of Devon Light Gloves because splits or holes may compromise sterility. The recall affects 559,108 kits distributed worldwide.
Product
Mini-Kits, Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description 31141479 K-1842-S OR Mini Kit 31141487 K-1560-S3 OR Mini Kit 31141495 K-1530-S3 OR Mini Kit 31141537 K-1940-S OR Mini Kit 31141552 K-1920-S OR Mini Kit 31141560 K-1200-S3 OR Mini Kit…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2179-2015·2015-07-29
FDA Recalls Fiber Stripper Tools Due to Sterilization Validation Issues
American Medical Systems is recalling 16,710 Fiber Stripper tools because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Product
Tool, Stripper W/BLD, 18S, Autoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2162-2015·2015-07-29
FDA Recalls Sure F!ex Reusable Lithotripsy Fibers Due to Sterilization Validation Issues
American Medical Systems is recalling 16,710 Sure F!ex reusable laser fibers because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Product
200¿M Lithotripsy Fiber- Reusable; Sure F!ex laser fibers are intended for use in laser-based surgical applications, including, but not limited to endoscopic, laparoscopic and open surgical procedures involving vaporization, ablation, coagulation, hemostasis, excision…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V476000·2015-07-29
Ford Recalls 2015 Lincoln MKT Vehicles Missing Second Row Seats
Ford is recalling 2015 Lincoln MKT vehicles delivered without second-row seats, creating a safety compliance issue and increased crash injury risk.
Product
LINCOLN — LINCOLN MKT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2134-2015·2015-07-29
Volcano Intravascular Ultrasound Systems Recalled for Inaccurate FFR/iFR Values
Volcano Corporation is recalling s5/s5i/CORE Intravascular Ultrasound Systems due to a software issue that may cause inaccurate FFR/iFR values.
Product
Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3 and 3.4 (with and without iFR Scout Technology) and v.3.4 software kits; Model s5i Radiology: The Volcano s5/s5i and CORE Series Intravascular Imaging and Pressure System is used for the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2122-2015·2015-07-29
GE Healthcare Precision RXi Digital System Monitor Suspension Recall
GE Healthcare is recalling Precision RXi Digital systems because a monitor fell from its suspension, posing an injury risk to patients or operators.
Product
GE Healthcare Precision RXi Digital system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2117-2015·2015-07-29
FDA Recalls Non-Sterile Devon Light Gloves Due to Splits and Holes
The FDA is recalling non-sterile Devon Light Gloves because they contain splits or holes that compromise sterility. The recall affects lots with numbers beginning 508xxxx or lower.
Product
NS-3600-B LITE GLOVE 1000/CASE -Bulk, Non-sterile Catalog Number: 571711
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2132-2015·2015-07-29
Volcano Intravascular Ultrasound Systems Recalled for Inaccurate FFR/iFR Values
Volcano Corporation is recalling s5, s5i, and CORE Intravascular Ultrasound Systems due to a software issue that may calculate inaccurate FFR/iFR values.
Product
Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3 and 3.4 (with and without iFR Scout Technology) and v.3.4 software kits; Model s5x. Radiology: The Volcano s5/s5i and CORE Series Intravascular Imaging and Pressure System is used for the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2102-2015·2015-07-29
Stryker SelectCore Biopsy Device Recalled for Stylet Ejection Risk
Stryker is recalling 55 units of the SelectCore Variable Throw Biopsy Device because the stylet may eject during use.
Product
Stryker SelectCore Variable Throw Biopsy Device, 14G, 10CM Product Usage: The Stryker SelectCore Variable Throw Biopsy Device is used in obtaining biopsy samples from soft tissues such as liver, breast, kidney, prostate, spleen, lymph nodes, and various soft tissue tumors.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2097-2015·2015-07-29
Maquet Magnus Hybrid OR Table Column Recalled for Collision Risk
Maquet is recalling 12 Magnus Hybrid OR Table Columns due to a potential collision risk with the C-arm of the Siemens Artis Zeego Angiography System.
Product
Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Siemens Artis Zeego Angiography System. Maquet GmbH & Co.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2199-2015·2015-07-29
Philips Recalls GEMINI TF Big Bore CT/PET Systems Due to Software Defects
Philips is recalling 44 GEMINI TF Big Bore CT/PET systems worldwide because four software defects in the Tumor LOC application may cause incorrect tissue irradiation.
Product
GEMINI TF Big Bore CT/PET System. The Philips GEMINI PET/CT Imaging Systems are a family of integrated diagnostic X-ray Computed Tomography (CT) and Positron Emission Tomography (PET) systems suitable for a wide range of diagnostic applications.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2133-2015·2015-07-29
Volcano Intravascular Ultrasound Systems Recalled for Inaccurate FFR/iFR Values
Volcano Corporation is recalling Volcano s5/s5i/CORE Intravascular Ultrasound Systems due to a software issue that may cause inaccurate FFR/iFR values.
Product
Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3 and 3.4 (with and without iFR Scout Technology) and v.3.4 software kits; Model CORE Mobile. Radiology: The Volcano s5/s5i and CORE Series Intravascular Imaging and Pressure System is used for the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2178-2015·2015-07-29
FDA Recalls Fiber Stripper Tools Due to Cleaning Validation Issues
American Medical Systems is recalling 16,710 Fiber Stripper tools because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Product
Tool, Stripper W/BLD, 18S, Nonautoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2176-2015·2015-07-29
FDA Recalls American Medical Systems Fiber Stripper Tools Due to Sterilization Issues
American Medical Systems is recalling Fiber Stripper tools because their cleaning and sterilization instructions do not meet FDA guidance for reusable medical devices.
Product
Tool, Stripper W/BLD, 14S, Nonautoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2153-2015·2015-07-29
Bausch & Lomb SofPort Advanced Optics Aspheric Lens Recall for Haptic Breakage
Bausch & Lomb is recalling SofPort Advanced Optics Aspheric Lenses because haptics may break during loading and insertion.
Product
Bausch & Lomb SofPort Advanced Optics Aspheric Lens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2202-2015·2015-07-29
Abbott ARCHITECT c8000 System Recalled for Tubing Leak Risk
Abbott Laboratories is recalling five ARCHITECT c8000 systems because the tubing may not meet specifications and could leak.
Product
ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott ARCHITECT cSystem is intended for In Vitro diagnostic use only. It is designed to perform automated: chemistry tests, utilizing photometry and potentiometric technology.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2106-2015·2015-07-29
FDA Recalls Sterile Devon Light Gloves Due to Splits and Holes
The FDA is recalling sterile Devon Light Gloves because splits or holes compromise their sterility. The recall covers 26,108,946 units distributed worldwide.
Product
Covidien Devon Light Gloves, Sterile-Single Units A disposable, sterile, single-use cover for compatible surgical light handles. Catalog/Number/Description 31140208 3611 LIGHT GLOVE 31140216 3613 LIGHT GLOVE 31140257 3612 LIGHT GLOVE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2121-2015·2015-07-29
GE Healthcare Precision RXi 23A/32A Analog System Monitor Suspension Recall
GE Healthcare is recalling Precision RXi 23A/32A Analog Systems because a monitor suspension failure could cause a monitor to fall and injure a patient or operator.
Product
GE Healthcare Precision RXi 23A/32A Analog System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2187-2015·2015-07-29
FDA Recalls Disposable EndoStat Fiber Strippers Due to Validation Deficiencies
American Medical Systems is recalling 16,710 disposable fiber strippers because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Product
Stripper, 0.2mm Disposable EndoStat Fiber, The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2120-2015·2015-07-29
GE Healthcare Precision 500D Monitor Suspension Recall
GE Healthcare is recalling Precision 500D and related fluoroscopic systems because monitor suspensions may fail, posing a risk of injury to patients or operators.
Product
GE Healthcare Precision 500D Classical R & F system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2112-2015·2015-07-29
Surgical Kits Recalled Due to Glove Splits Compromising Sterility
The FDA is recalling 114,813 surgical kits containing Devon Light Gloves due to splits or holes that compromise sterility.
Product
Surgical Kit Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description: 573326 7497-HLS Surgical Kit 573328 7437-NRF SURGICAL ASC KIT 573343 7499-88 SURGICAL KIT with Light Gloves 573346 7499-TLG Surgical Kit with Edge 573359 7499-HLW Surgical KIT 573368…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2135-2015·2015-07-29
Volcano Intravascular Ultrasound Systems Recalled for Inaccurate FFR/iFR Values
Volcano Corporation is recalling specific software versions for its s5 and CORE Intravascular Ultrasound Systems because they may calculate inaccurate FFR/iFR values under certain circumstances.
Product
Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3 and 3.4 (with and without iFR Scout Technology) and v.3.4 software kits; Model s5ix/s5iz Radiology: The Volcano s5/s5i and CORE Series Intravascular Imaging and Pressure System is used for the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2167-2015·2015-07-29
American Medical Systems Recalls Fiber Stripper Due to Sterilization Validation Issues
American Medical Systems is recalling 16,710 Fiber Strippers because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Product
Fiber Stripper, 365¿m, Autoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes, corresponding…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V474000·2015-07-29
Harley-Davidson Recalls 2015 XG500 and XG750 Motorcycles for Fuel Pump Defect
Harley-Davidson is recalling 2015 XG500 and XG750 motorcycles because a poor fuel pump seal may interrupt fuel supply, causing abrupt power restoration and loss of control.
Product
HARLEY-DAVIDSON — HARLEY-DAVIDSON XG500, XG750
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2109-2015·2015-07-29
Minor Surgical Kits Recalled Due to Sterility Compromise in Gloves
FDA is recalling Minor Surgical Kits containing Devon Light Gloves with splits or holes that compromise sterility.
Product
Minor Surgical Kits, Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description: 573208 7519-DHCG MINOR KIT 573210 7581-CSD Minor KIT 573741 7667-HMI Minor Kit 31144507 7519 Minor Surgical Kit 573830D MINOR KIT
Category
Medical Device
Distribution
Distributed nationwide