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.

31351–31375 of 76775

HighFDA (Devices)·Z-0978-2020·2020-02-12
Cook Inc. Recalls Universa Soft Ureteral Stents Due to Wire Guide Loading Error
Cook Inc. is recalling Universa Soft Ureteral Stents because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Product
Universa Soft Ureteral Stent, Global Product No. G49887 G49933 G49934 G49937 G49940 G49941 G49942 G49945 G49947 G49948 G49949 G49950 G49951 G49953 G49955 G49956 G49957 G49958 G49959 G49961 G53145 G53676 G53677 G53687 G53689 G53692 G53693 G53694 G53703…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0968-2020·2020-02-12
Cook Inc. Recalls Percutaneous Malecot Nephrostomy Sets Due to Wire Guide Loading Error
Cook Inc. is recalling 13,388 Percutaneous Malecot Nephrostomy Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Product
Percutaneous Malecot Nephrostomy Set, Global Product No. G16714 G19107 G19108
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1033-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination
Cardinal Health is recalling AAMI 3 Non-Reinf Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 NON-REINF SURGICAL GOWN XL, Item Code 9545
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0997-2020·2020-02-12
Roche Recalls Accu-Chek Aviva Plus Blood Glucose Test Strips
Roche Diabetes Care is recalling Accu-Chek Aviva Plus test strips because they may fail to dose, potentially delaying treatment decisions.
Product
Accu-Chek Aviva Plus Health Network Strips- intended for Blood Glucose Monitoring System Catalog Number: 06908349001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0959-2020·2020-02-12
Cook Inc. Recalls Bentson PTFE Wire Guides Due to Loading Error
Cook Inc. is recalling Bentson PTFE Wire Guides because they may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Product
Bentson PTFE Wire Guide, Guidewire, Global Product Number G14589, G14590
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1001-2020·2020-02-12
Medonic M-Series Hematology Analyzer Recalled for Sample Misidentification and Needle Injury Risk
Clinical Diagnostic Solutions is recalling Medonic M-Series Hematology Analyzers due to a risk of sample misidentification and operator injury from exposed needles.
Product
Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075; OUS Product code 1400011
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0975-2020·2020-02-12
Cook Inc. Recalls Sof-Flex Double Pigtail Ureteral Stent Sets
Cook Inc. is recalling Sof-Flex Double Pigtail Ureteral Stent Sets because the wire guide may be incorrectly loaded, potentially introducing a stiff tip into the patient.
Product
Sof-Flex Double Pigtail Ureteral Stent Set, Global Product No. G15076 G14906 G14840 G14865 G17128
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0974-2020·2020-02-12
Cook Inc. Recalls Kwart Retro-Inject Ureteral Stent Sets
Cook Inc. is recalling Kwart Retro-Inject Ureteral Stent Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient instead of the flexible tip.
Product
Kwart Retro-Inject Ureteral Stent Set, Global Product No. G15016 G14836 G14885 G14887 G17151
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0935-2020·2020-02-12
B. Braun Outlook Safety Infusion System Y-type Blood Set Recall for Leakage
B. Braun Medical is recalling 1,824 Outlook Safety Infusion System Y-type Blood Sets due to a potential for leakage at the joint between the blood filters and tubing.
Product
Outlook Safety Infusion System Y-type Blood Set, Catalog Number 477005
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1064-2020·2020-02-12
Centurion Medical Recalls Sterile Surgical Trays Due to Incomplete Seals
Centurion Medical Products Corporation is recalling specific sterile surgical trays because incomplete seals may compromise sterility. The affected products were distributed nationwide and in Ghana.
Product
Centurion-Surgical trays DYNJ04079Z CIRCUMCISION TRAY STERILE DYNJ08835 DEBRIDEMENT TRAY W/SAFETY SCAL DYNJ1000 NEWBORN CIRCUMCISION TRAY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0939-2020·2020-02-12
B. Braun Recalls Y-Type Blood Sets Due to Leakage Risk
B. Braun Medical is recalling 9,000 Y-Type Blood Sets because of a potential for leakage at the joint between the blood filters and tubing.
Product
Y-Type Blood Set, Catalog Number 490530
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1006-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels
Cardinal Health is recalling specific lots of AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 FABRNF SCRUB SURG GWN XL NS, Gown. Item Code 91070NB
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1065-2020·2020-02-12
Centurion Incision and Drainage Trays Recalled for Incomplete Seals
Centurion Medical Products is recalling specific Incision and Drainage Trays because incomplete seals may compromise sterility.
Product
Centurion-Incision /Drainage Tray ID1235A ESKENAZI INCISION & DRAINAGE TRAY ID1525 INCISION & DRAINAGE TRAY ID1670 I&D TRAY ID1715 INCISION & DRAINAGE TRAY ID1765 ER I&D PACK ID1765 ER I&D PACK ID1835 I & D TRAY ID2075 I&D TRAY ID585 INCISION & DRAINAGE TRAY ID875…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1017-2020·2020-02-12
Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination Levels
Cardinal Health is recalling AAMI 3 fabric-reinforced surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.
Product
AAMI 3 FABRIC REINF SURG GOWN XL NS, Item Code 9541NA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0987-2020·2020-02-12
Cocoon Convective Warming System Recalled for Thermal Damage Risk
Care Essentials is recalling 251 Cocoon Convective Warming Systems due to a potential for thermal damage near the power cord connector and Power Entry Module.
Product
Cocoon Convective Warming System, Product Code: CWS5000 (110V).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0971-2020·2020-02-12
Cook Inc. Recalls Urethral Dilator Sets Due to Wire Guide Loading Error
Cook Inc. is recalling Urethral Dilator Sets because the wire guide may load incorrectly, causing a stiff tip to be introduced into the patient instead of a flexible one.
Product
Urethral Dilator Set, Global Product No. G14185
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0986-2020·2020-02-12
Cocoon Convective Warming System Recalled for Thermal Damage Risk
Care Essentials is recalling 689 Cocoon Convective Warming Systems due to a risk of thermal damage near the power cord connector and Power Entry Module.
Product
Cocoon Convective Warming System, Product Code: CWS4000 (110V).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1066-2020·2020-02-12
Centurion Tracheostomy Care Kits Recalled Due to Incomplete Package Seals
Centurion Medical Products is recalling specific tracheostomy care kits because incomplete seals on the sterile packaging may compromise sterility.
Product
Centurion- Trach Kits TC6282G TRACHEOSTOMY CARE TRAY TC7170 LATEX FREE TRACHEOSTOMY CARE TRAY TC7370 TRACHEOSTOMY KIT TC7450 DISPOSABLE TRACH TRAY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0977-2020·2020-02-12
Cook Inc. Recalls Universa Firm Ureteral Stents Due to Loading Error
Cook Inc. is recalling Universa Firm Ureteral Stents because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient instead of the flexible tip.
Product
Universa Firm Ureteral Stent, Global Product No. G49864 G49865 G49866 G49867 G49868 G49869 G49870 G49874 G49875 G49877 G49879 G49881 G49882 G49887 G49888
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0961-2020·2020-02-12
Cook Inc. Recalls Heavy Duty PTFE Wire Guides Due to Loading Error
Cook Inc. is recalling 146 Heavy Duty PTFE Wire Guides because they may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.
Product
Heavy Duty PTFE Wire Guide, Guidewire, Global Product Number G14323 G14260 G14260
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1050-2020·2020-02-12
Centurion Pelvic Exam Kits Recalled for Incomplete Sterile Seals
Centurion Medical Products is recalling specific lots of Pelvic Exam Kits because incomplete seals may compromise sterility.
Product
Centurion- Pelvic Exam Kits DYNDE1037 PELVIC EXAM TRAY,UNIVERSITY H 2019032090 DYNDE1037 PELVIC EXAM TRAY,UNIVERSITY H 2018091790
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1054-2020·2020-02-12
Centurion Medical Products Recalls Surgical Trays Due to Incomplete Seals
Centurion Medical Products is recalling various surgical trays and kits because incomplete seals on the sterile packages may compromise sterility.
Product
Centurion-Surgical Tray MNS10255 DELIVERY TRAY MNS10255 DELIVERY TRAY MNS10310 MEATOTOMY TRAY MNS10310 MEATOTOMY TRAY MNS10525 DELIVERY INSTRUMENT TRAY MNS10620 PACEMAKER TRAY MNS10820 ENT/EPISTAXIS KIT MNS10920 PODIATRY NAIL PACK MNS10985 CERCLAGE REMOVAL KIT MNS11020…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1077-2020·2020-02-12
Centurion Medical Valve Change Kit Recalled for Incomplete Sterile Seals
Centurion Medical Products Corporation is recalling Valve Change Kits due to incomplete sterile package seals that may compromise sterility.
Product
Centurion-Trays EBSI1021 VALVE CHANGE KIT- DOUBLE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1059-2020·2020-02-12
Centurion Umbilical Vessel Catheter Recall Due to Incomplete Seals
Centurion Medical Products is recalling Umbilical Vessel Catheter Insertion devices due to incomplete sterile package seals that may compromise sterility.
Product
Centurion- Umbilical Vessel UPC175 UMBILICAL VESSEL CATH. INSERTION UPC175 UMBILICAL VESSEL CATH. INSERTION
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1063-2020·2020-02-12
Centurion Medical Recalls LVAD Kits Due to Incomplete Sterile Package Seals
Centurion Medical Products Corporation is recalling various LVAD kits because incomplete seals on the sterile package may compromise sterility.
Product
Centurion-LVAD Kits DM1005 DAILY LVAD MAINTENANCE KIT DM280A LVAD MANAGEMENT SYSTEM 2-7 DM320 PERCUTANEOUS LEAD MANAGEMENT KIT DM380 DAILY LVAD KIT MORRISTOWN MEDICAL DM405A ADVOCATE CHRIST DAILY WET KIT DM405A ADVOCATE CHRIST DAILY WET KIT DM525 LVAD SENSITIVE KIT DM545…
Category
Medical Device
Distribution
Distributed nationwide