State

Rhode Island product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38726–38750 of 76794

HighFDA (Devices)·Z-2873-2018·2018-08-29
GE Healthcare Optima CT660 Systems Recalled for Damaged Cable Hazard
GE Healthcare is recalling Optima CT660 systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Product
GE Healthcare Optima CT660. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. Sold only outside the U.S. under the following product names: CT OPTIMA 660, CT OPTIMA 660 LONG BJG SKD RUS, CT OPTIMA 660 LONG BJG SKD…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2840-2018·2018-08-29
Elekta Digital Accelerator Recall for Potential Uncontrolled Detector Arm Extension
Elekta is recalling 2,998 Digital Accelerators worldwide due to a potential for uncontrolled extension of iViewGT or XVI detector arms.
Product
ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise Digital Accelerator, Infinity, Axesse, and Versa HD
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18763·2018-08-29
BSN Sports Recalls Rubber Critter Toys for Lead Paint Violation
BSN Sports is recalling rubber critter toys because the orange and yellow paint contains lead levels exceeding federal bans. No injuries have been reported.
Product
Rubber critter toys
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2858-2018·2018-08-29
Philips DigitalDiagnost Dual Detector Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost Dual Detector units because the footplate hook may fail, causing the plate to fall and injure patients or operators.
Product
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2854-2018·2018-08-29
Philips DigitalDiagnost 4.1 Flex Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost 4.1 Flex and Value units because the footplate hook may fail, causing the footplate to fall and injure patients or operators.
Product
DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2870-2018·2018-08-29
GE Healthcare Recalls CT Systems Due to Damaged Cable Electrical Hazard
GE Healthcare is recalling specific CT systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Product
GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. Sold under the following product names: CT GOLDSEAL LIGHTSPEED ULTRA, CT OPTIMA 660, CT OPTIMA…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2864-2018·2018-08-29
Philips DigitalDiagnost Upgrades Recalled Due to Footplate Safety Hazard
Philips is recalling DigitalDiagnost Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Upgrades (Stitching Patient Support) 712083
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2853-2018·2018-08-29
Philips DigitalDiagnost 4.1 Chest X-Ray Unit Recalled for Footplate Hazard
Philips is recalling DigitalDiagnost 4.1 Chest X-Ray units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.
Product
DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2868-2018·2018-08-29
Philips EasyDiagnost Eleva DRF Footplate Hook Recall
Philips is recalling EasyDiagnost Eleva DRF units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2859-2018·2018-08-29
Philips DigitalDiagnost Dual Detector Footplate Recall for Injury Risk
Philips is recalling DigitalDiagnost Dual Detector units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2867-2018·2018-08-29
Philips EasyDiagnost Eleva DRF Footplate Recall for Injury Risk
Philips is recalling EasyDiagnost Eleva DRF units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
EasyDiagnost Eleva DRF (Stitching Patient Support) 706032
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2845-2018·2018-08-29
Philips DigitalDiagnost Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost Release 3.1 units because a defective hook allows the footplate to fall or swing, posing an injury risk to operators or patients.
Product
DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2841-2018·2018-08-29
Philips DigitalDiagnost 2.x Upgrades Recalled Due to Footplate Injury Risk
Philips is recalling two DigitalDiagnost 2.x Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to operators or patients.
Product
DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2872-2018·2018-08-29
GE Healthcare Optima CT540 Systems Recalled for Damaged Cable Hazard
GE Healthcare is recalling Optima CT540 systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.
Product
GE Healthcare Optima CT540. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.Sold under the following product names: BEIJING CT OPTIMA 540, BEIJING OPTIMA, BEIJING OPTIMA 540, BEIJING OPTIMA 540 ASIR, CT BEIJING…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2862-2018·2018-08-29
Philips DigitalDiagnost Footplate Hook Recall Due to Injury Risk
Philips is recalling DigitalDiagnost Release 3.1 units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2752-2018·2018-08-29
Handicare C Series Patient Lifts Recalled for Premature Strap Wear
Handicare USA Inc. is recalling 716 C Series Patient Lifts because straps may wear and break prematurely at maximum weight conditions.
Product
Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2856-2018·2018-08-29
Philips DigitalDiagnost Classic 1.x Upgrades Recalled for Footplate Safety Hazard
Philips is recalling DigitalDiagnost Classic 1.x Upgrades because the footplate hook may fail to hold the plate securely, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2887-2018·2018-08-29
CAREstream ProNox Nitrous Oxide Delivery Systems Recalled for High Gas Levels
CAREstream Medical LLC is recalling 919 ProNox Nitrous Oxide Delivery Systems because two units delivered higher levels of nitrous oxide than specified during routine testing.
Product
CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b. CMI-0100-PNX-HS, Pro-Nox Complete Hospital Roll Stand System - Nitrous Oxide Delivery System; c. CMI-0100-PNX-HS-NO2H, Pro-Nox Hospital System…
Category
Medical Device
Distribution
47 states
HighFDA (Devices)·Z-2855-2018·2018-08-29
Philips DigitalDiagnost 4.1 High Performance Footplate Recall Issued
Philips is recalling DigitalDiagnost 4.1 High Performance units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2852-2018·2018-08-29
Philips DigitalDiagnost 4.1 Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost 4.1 units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.
Product
DigitalDiagnost 4.1 (Stitching Patient Support) 712225
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2851-2018·2018-08-29
Philips DigitalDiagnost 4 Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost 4 High Performance units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2863-2018·2018-08-29
Philips DigitalDiagnost Single Detector Footplate Hook Recall
Philips is recalling DigitalDiagnost Single Detector units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Product
DigitalDiagnost Single Detector (Stitching Patient Support) 712020
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2865-2018·2018-08-29
Philips DigitalDiagnost Dual-Detector Recall for Footplate Safety Hazard
Philips is recalling DigitalDiagnost Dual-Detector units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost, Dual-Detector (Stitching Patient Support) 712052
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2846-2018·2018-08-29
Philips BuckyDiagnost Ceiling System Recalled for Footplate Safety Hazard
Philips is recalling BuckyDiagnost Ceiling Systems because the footplate hook may fail to hold the plate securely, posing a risk of injury to patients or operators.
Product
BuckyDiagnost Ceiling System (Stitching Patient Support) 704031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2857-2018·2018-08-29
Philips DigitalDiagnost Classic Footplate Hook Recall for Injury Risk
Philips is recalling DigitalDiagnost Classic units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Product
DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052
Category
Medical Device
Distribution
Distributed nationwide