State

Rhode Island product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57901–57925 of 76887

HighFDA (Devices)·Z-0887-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender I 17/80 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections through…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0883-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK¿ Tender I 13/60 10 pieces Product Usage: Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0876-2015·2015-01-07
Bard Caliber Inflation Device Recalled for Pressure Limitations
Perouse Medical is recalling Bard Caliber inflation devices that may fail to reach required pressure, potentially delaying angioplasty procedures.
Product
Bard Caliber (CL3030) Inflation Device Product Usage: Inflation Device intended for use during cardiovascular to create and maintain, monitor pressure in the balloon catheter - balloon inflation device for angioplasty procedures
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0898-2015·2015-01-07
Smiths Medical Recalls Hypodermic Needles Due to Safety Sheath Failure
Smiths Medical ASD, Inc. is recalling specific lots of Needle Pro Edge safety hypodermic needles because the needle is not captured in the safety sheath.
Product
Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 10mL Luer lock syringe; Reorder Number: 4102010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0895-2015·2015-01-07
Atricure CryoICE Cryogenic Probe Recalled for Potential Sterility Compromise
Atricure Inc is recalling 19,190 CryoICE cryogenic probes due to packaging defects that may have compromised sterility.
Product
Cryogenic probe for cardiac ablation surgery, packaged individually in Tyvek pouches Product Usage: Cryogenic probe for cardiac ablation surgery. The CryoICE cryoablation probe is a sterile, single use device intended to use in the cryosurgical treatment of cardiac…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0897-2015·2015-01-07
Smiths Medical Needle Pro Edge Safety Device Recall for Uncaptured Needles
Smiths Medical ASD, Inc. is recalling specific lots of Needle Pro Edge Safety Devices because the needle is not captured in the safety sheath.
Product
Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0894-2015·2015-01-07
ACCU-CHEK Tender II Infusion Sets Recalled for Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender II infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender II 17/110 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0888-2015·2015-01-07
Roche Recalls ACCU-CHEK Tender I Infusion Sets Due to Tubing Detachment Risk
Roche Diagnostics is recalling ACCU-CHEK Tender I infusion sets because the tubing may detach, interrupting insulin delivery without an alarm.
Product
ACCU-CHEK Tender I 17/110 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0877-2015·2015-01-07
Perouse Medical Recalls Synthes Inflation System Due to Pressure Limitations
Perouse Medical is recalling 2,184 units of the Synthes Inflation System because the device may fail to raise pressure above 10 atm, potentially delaying procedures.
Product
Synthes Inflation System (03.804.4135) Product Usage: Inflation system is used during kyphoplasty or other interventional kyphoplasty or other interventional procedures, to create and monitor pressure In the balloon catheter and pressure In the balloon catheter and to to…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V001000·2015-01-05
MCI Recalls J4500 Motor Coaches Due to Brake Hose Wear Risk
Motor Coach Industries is recalling 2013-2015 MCI J4500 motor coaches because a brake hose may rub against the tire or control arm, potentially causing a loss of braking power.
Product
MCI — MCI J4500
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0868-2015·2014-12-31
Halyard Health Recalls KimVent Microcuff Endotracheal Tubes Due to Detachment Risk
Halyard Health is recalling KimVent Microcuff Subglottic Suctioning Endotracheal Tubes because the cuff inflation line may detach during use.
Product
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 8.5 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0585-2015·2014-12-31
Heart Sync Defibrillation Electrodes Recalled for Incompatibility with Philips AEDs
Heart Sync, Inc. is recalling Adult Radiotranslucent Electrodes because they do not connect with Philips FR3 or FRx AED units, potentially preventing defibrillation.
Product
ADULT Radiotranslucent Electrode, Part number T100LO-PHILIPS, Rx ONLY, For use with Philips HeartStart AED "Comparable to Philips Medical HeartStart Electrodes Plug Style Connector", Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring, Single use.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0867-2015·2014-12-31
Halyard Health Recalls KimVent Microcuff Endotracheal Tubes Due to Detachment Risk
Halyard Health is recalling KimVent Microcuff Endotracheal Tubes because the cuff inflation line may detach during use, potentially compromising airway management.
Product
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 8.0 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·14V830000·2014-12-31
Subaru Recalls Brake Line Corrosion in Impreza, WRX, and Forester Models
Subaru is recalling specific Impreza, WRX, STI, and Forester vehicles to fix brake line corrosion that could cause fluid leaks and increased stopping distances.
Product
SUBARU — SUBARU WRX, FORESTER, IMPREZA, WRX STI
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0587-2015·2014-12-31
Heart Sync Electrodes Recalled for Incompatibility with Philips AEDs
Heart Sync, Inc. is recalling multi-function defibrillation electrodes that do not connect with Philips FR3 or FRx AED units, potentially preventing proper device operation.
Product
ADULT/CHILD Radiotranslucent Electrode, Part number T100AC-PHILIPS, Rx ONLY, For use with Philips HeartStart AED "Comparable to Philips Medical HeartStart Electrodes Plug Style Connector", Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring, Single…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0584-2015·2014-12-31
Heart Sync Defibrillation Electrodes Recalled for Incompatibility with Philips AEDs
Heart Sync, Inc. is recalling Adult/Child Radiotransparent Electrodes because they do not connect with Philips FR3 or FRx AED units, potentially preventing defibrillation.
Product
ADULT/CHILD Radiotransparent Electrode, Part number C100AC-PHILIPS, Rx ONLY, For use with Philips HeartStart AED "Comparable to Philips Medical HeartStart Electrodes Plug Style Connector", Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring, Single…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0324-2015·2014-12-31
Hospira Recalls Heparin Sodium Injection Due to Human Hair Particulate
Hospira is recalling 63,378 units of Heparin Sodium injection because human hair was found sealed inside the container's administration port.
Product
HEPARIN SODIUM — HEPARIN SODIUM (HEPARIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereUSDA FSIS·093-2014·2014-12-31
Campos Foods Recalls Chicken Products Due to Undeclared Peanuts
Campos Foods is recalling approximately 5,300 pounds of chicken products because they contain undeclared peanuts, a known allergen.
Product
Tennessee Firm Recalls Chicken Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0865-2015·2014-12-31
Halyard KimVent Endotracheal Tubes Recalled for Cuff Line Detachment Risk
Halyard Health is recalling KimVent Microcuff Subglottic Suctioning Endotracheal Tubes because the cuff inflation line may detach during use.
Product
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0869-2015·2014-12-31
Halyard Health Recalls KimVent Microcuff Endotracheal Tubes Due to Detachment Risk
Halyard Health is recalling KimVent Microcuff Subglottic Suctioning Endotracheal Tubes because the cuff inflation line may detach during use.
Product
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 9.0 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0866-2015·2014-12-31
Halyard KimVent Endotracheal Tubes Recalled for Cuff Line Detachment
Halyard Health is recalling KimVent Microcuff Endotracheal Tubes because the cuff inflation line may detach from the tube during use.
Product
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.5 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0583-2015·2014-12-31
Heart Sync Electrodes Recalled for Incompatibility with Philips AEDs
Heart Sync, Inc. is recalling Adult Radiotransparent Electrodes that fail to connect with Philips FR3 or FRx AED units, potentially preventing defibrillation.
Product
ADULT Radiotransparent Electrode, Part number C100-PHILIPS, Rx ONLY, For use with Philips HeartStart AED "Comparable to Philips Medical HeartStart Electrodes Plug Style Connector", Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring, Single use.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0848-2015·2014-12-31
Ortho-Clinical Diagnostics Recalls VITROS TRIG Slides Due to Biased Results
Ortho-Clinical Diagnostics is recalling specific VITROS TRIG slides due to a potential for biased test results. The recall affects 380 units in the US and 155 units internationally.
Product
VITROS CHEMISTRY PRODUCTS TRIG Slides, REF 133 6544, IVD For in vitro diagnostic use only. VITROS Chemistry Products TRIG Slides quantitatively measure triglyceride (TRIG) concentration in serum and plasma using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0586-2015·2014-12-31
Heart Sync Multi-function Defibrillation Electrodes Recalled for Incompatibility
Heart Sync, Inc. is recalling multi-function defibrillation electrodes that do not connect with Philips FR3 or FRx AED units, potentially preventing proper use.
Product
ADULT Radiotranslucent Electrode, Part number T100-PHILIPS, Rx ONLY, For use with Philips HeartStart AED "Comparable to Philips Medical HeartStart Electrodes Plug Style Connector", Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring, Single use.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0802-2015·2014-12-31
GE Healthcare Pediatric Defibrillation Electrodes Recalled for Arcing Risk
Leonhard Lang GmbH is recalling GE Healthcare Pediatric Defibrillation Electrodes because arcing may cause malfunction, delaying or preventing life-saving therapy.
Product
GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing Electrodes. REF 2059144-001 and 2059144-005. . Product Usage: Usage: Skintact Pediatric Multifunction Electrodes are for use on pediatric patients, less than 8 years of age, or weighing less than 25 kg…
Category
Medical Device
Distribution
Distributed nationwide