State
73,576 recalls have nationwide distribution and so reach Rhode Island. 3,048 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,048 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 3,048 recalls whose distribution notice names Rhode Island specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
GE Healthcare is recalling Enterprise Archive V8 software because historical imaging data may be incorrectly associated with different patients, potentially leading to misdiagnosis.
Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
Philips North America is recalling 312 units of the PIC iX Essentials patient information system due to a software malfunction that may cause the system to freeze.
Howmedica Osteonics Corp. is recalling specific orthopaedic implant components manufactured with aged polyethylene material that may oxidize and increase wear.
GE Healthcare is recalling 116 Centricity PACS Server V7 systems because historical imaging data may be incorrectly associated with the wrong patient, potentially leading to misdiagnosis.
Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
Howmedica Osteonics Corp. is recalling specific orthopaedic implant components made from aged polyethylene. The material may oxidize and wear excessively, potentially causing device failure.
ICU Medical is recalling IV sets with drip chambers because black specks may be present in the fluid path due to a plastic molding issue.
GE Healthcare is recalling Centricity PACS software because historical imaging data may be incorrectly associated with different patients, potentially leading to misdiagnosis or delayed care.
GE Healthcare is recalling Centricity Enterprise Archive software because historical imaging data may be incorrectly associated with different patients, potentially leading to misdiagnosis or delayed care.
Howmedica Osteonics Corp. is recalling specific orthopaedic implant components because aged polyethylene material may cause increased wear and device failure.
Philips North America is recalling 7,359 Patient Information Center iX units due to a software malfunction that may cause the system to freeze and become unresponsive.
Maquet is recalling Percutaneous Insertion Kits because the packaging may not consistently maintain sterile barrier integrity.
restor3d Inc. is recalling two Kinos Axiom Total Ankle Systems because they were packaged with incorrect patient-specific cutting guides, which may lead to surgical complications.
Medline Industries is recalling 60 Myringotomy Pack-LF kits due to open seals that may compromise sterility and lead to patient infection.
Howmedica Osteonics Corp. is recalling specific orthopaedic implant components made with aged UHMWPE material. The material may oxidize, leading to increased wear, device fracture, or the need for revision surgery.
ICU Medical is recalling IV sets with drip chambers due to potential black specks and particulate matter in the fluid path.
Howmedica Osteonics Corp. is recalling specific Scorpio knee implant components due to aged polyethylene material that may cause increased wear and potential device failure.
Jaguar Land Rover is recalling one 2026 Range Rover Sport because a misaligned circuit board in the powertrain control module may cause loss of drive power.
NOXBOX LTD is recalling 1,547 NOxBOXi Nitric Oxide Delivery Systems due to potential oxygen tubing leaks that may cause oxygen desaturation.
Stryker is recalling 9,072 XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
ICU Medical is recalling IV sets with drip chambers due to potential black specks and particulate matter in the fluid path.
Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.
Maquet Cardiopulmonary GmbH is recalling Percutaneous Insertion Kits because packaging may not consistently maintain sterile barrier integrity.
Stryker is recalling XCEL Bladeless Trocars because the reusable access port system may crack or separate during use.