State
73,738 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.
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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Amneal Pharmaceuticals is recalling specific lots of Methylergonovine Maleate tablets because a Promethazine tablet was found in a bottle.
Pharma-Natural Inc. is recalling 3,000 bottles of GENCONTUSS cough syrup because it was manufactured with current good manufacturing practice violations.
Pharma-Natural Inc. is recalling 2,052 bottles of NEOGEN-D cough syrup because the product was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.
Abbott Laboratories is recalling 2,112 Apolipoprotein A1 assay kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Pharma-Natural Inc. is recalling LidoAID topical analgesic gel because it was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.
Pharma-Natural Inc. is recalling 7,392 bottles of SORBUGEN cough syrup because the product was manufactured with current good manufacturing practice violations.
Abbott Laboratories is recalling 5,694 Haptoglobin Assay kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Siemens is recalling 39 AXIOM Artis dFA units because a power supply issue may cause generator failure, preventing X-ray production during procedures.
Deva Holding AS is recalling Temozolomide capsules because manufacturing deviations allowed possible cross-contamination with beta-lactam products.
Pharma-Natural Inc. is recalling Tusslin cough syrup because it was manufactured with current good manufacturing practice violations, including a lack of process validation.
Siemens is recalling one AXIOM Artis dBC X-ray system because a power supply defect may prevent X-ray generation during procedures.
Siemens Medical Solutions is recalling three Artis zee biplane MN units due to a power supply tolerance issue that may prevent X-ray generation during procedures.
Siemens is recalling four AXIOM Artis FA units due to a power supply tolerance issue that may cause generator failure and prevent X-ray imaging.
Pharma-Natural Inc. is recalling 998 bottles of Oliver's Harvest CBD+Capsaicin 0.2% Pain Relief Cream due to current good manufacturing practice violations.
Pharma-Natural Inc. is recalling 1,000 jars of Dayma SUPER FORTE XL10 Pain Relieving Topical Analgesic Gel due to current good manufacturing practice violations.
Siemens is recalling seven AXIOM Artis BA X-ray systems because a power supply defect may cause the generator to fail, preventing X-ray imaging.
Abbott Laboratories is recalling 8,132 C3 in vitro diagnostic kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Abbott Laboratories is recalling 5,483 units of ARCHITECT BNP Calibrators worldwide due to a time-dependent stability drift that affects patient and control test results.
Pharma-Natural Inc. is recalling Army Health Pain Reliever Gel with Curcumin because it was manufactured with current good manufacturing practice violations.
Medela Inc is recalling 665,600 breast milk transfer lids because packaging breaches may compromise sterility, even if the packaging appears intact.
Merge Healthcare is recalling 73 units of Merge OrthoPACS software due to potential display errors in image ordering and scrolling.
Siemens is recalling five AXIOM Artis TA units due to a power supply tolerance issue that can cause generator failure and prevent X-ray imaging.
Siemens is recalling six AXIOM Artis BC units because a power supply tolerance issue may cause the X-ray generator to fail during procedures.
Pharma-Natural Inc. is recalling Dermanak Skin Fade Cream because it was manufactured with current good manufacturing practice violations.
Siemens is recalling 53 AXIOM Artis dBC units due to a power supply tolerance issue that can cause generator failure and prevent X-ray imaging.