State
73,824 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.
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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hartley Medical Center Pharmacy is recalling Hydromorphone HCL 0.5 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Hartley Medical Center Pharmacy is recalling specific syringes of Hydromorphone and Bupivacaine due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling specific syringes of Sufentanil Citrate and Clonidine HCL due to a lack of assurance of sterility.
Arrow International is recalling UltraFlex IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate 11 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Abbott Vascular is recalling the MitraClip Clip Delivery System because a mandrel fracture may prevent the clip from detaching during implantation.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and baclofen syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate 0.5 mg/ml syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Hydromorphone HCL and Bupivacaine HCL syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and fentanyl syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Baclofen 2000 mcg/ml syringes because the agency could not ensure the product was sterile.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Bupivacaine HCL syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling two syringes of Morphine Sulfate 1.5 mg/ml due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Hydromorphone HCL 10 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Arrow International is recalling specific Percutaneous Insertion Trays because the sheath body may separate from the hub, posing a risk of bleeding.
Hartley Medical Center Pharmacy is recalling Hydromorphone HCL 2 mg/ml syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Sufentanil Citrate/Clonidine/Bupivacaine syringes because the agency could not ensure the product was sterile.
Mack is recalling 2016-2017 Titan trucks because a steering shaft bolt may fail, causing loss of steering and potential crashes.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate 20 mg/ml syringes due to a lack of assurance of sterility. The product was distributed nationwide.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate, Sufentanil Citrate, and Bupivacaine HCL vials due to a lack of assurance of sterility.
Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.
Philips Respironics is recalling approximately 104,508 Trilogy and Garbin ventilators due to a software issue. The recall covers units distributed nationwide and internationally.
Sedecal S.A. is recalling 349 mobile X-ray systems because static electricity and other issues can cause uncommanded movements.
SRAM is recalling Zipp 88 aluminum front hubs because the flanges can fail, posing a crash and injury hazard. Consumers should stop using the hubs and contact SRAM for a free replacement.
Arrow International Inc. is recalling Super Arrow-Flex Percutaneous Sheath Introducer Sets because packaging damage may compromise sterility, posing a potential infection risk.