State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Coviden is recalling specific sterile Foley catheter trays because the temperature sensors may display lower body temperature readings than the patient's actual temperature.
Degania Silicone is recalling 250 Foley Temperature Sensor Catheters because defective sensors may display lower body temperatures than the patient's actual temperature.
Degania Silicone is recalling 14,326 Thermistor Foley catheters because defective sensors may display inaccurate, lower body temperature readings.
Degania Silicone is recalling 16,133 temperature sensor catheters because defective sensors may display lower body temperatures than the patient's actual temperature.
Degania Silicone is recalling Foley catheters with temperature sensors because defective units may display lower body temperatures than actual.
Covidien is recalling P400 temperature sensor catheters because they may display lower body temperature readings than the patient's actual temperature.
BMW is recalling 2013-2015 760Li vehicles because incompatible software in the Engine Control Unit may cause the engine to stall, increasing crash risk.
Baxter Healthcare is voluntarily recalling 5,184 bags of 0.9% Sodium Chloride Injection USP 50 mL due to a cGMP deviation. The FDA classified this as a Class II recall.
Coviden is recalling Temp Sense Silicone catheters because they may display lower body temperature measurements than the patient's actual temperature.
Beaumont Bio-Med, Inc. is recalling 160 bottles of Diarrhea Response Homeopathic Formula due to manufacturing deviations that could result in microbial contamination.
Arrow International is recalling 5.5 Fr x 5.5 Fr x 40 cm double-lumen PICC Kits because they may contain the wrong catheter type, potentially delaying treatment.
Tecan US, Inc. is recalling Freedom EV0-2 devices with EVOware Sample Tracking Add-On V1.0 or higher due to a software issue that can impact sample identification and traceability.
Biocare Medical is recalling 11 URO-3 Triple Stain kits because two components were mislabeled, causing incorrect staining patterns in laboratory tests.
Beaumont Bio-Med is recalling Sore Throat & Laryngitis Response Homeopathic Formula due to manufacturing deviations that could result in microbial contamination.
Siemens is recalling 429 ARTIS Pheno Interventional Fluoroscopic X-Ray Systems because a temperature control defect may cause the detector to cool below its designed operating range.
Torrent Pharma Inc. is recalling 15,384 bottles of Lamotrigine Extended-Release Tablets, 200 mg, because they failed dissolution testing during stability checks.
Arrow International is recalling specific PICC kits because they may contain the wrong catheter type, potentially delaying patient treatment.
Beaumont Bio-Med is recalling 140 bottles of Arthritis Pain Relief Homeopathic Formula due to manufacturing conditions that could result in microbial contamination.
bioMerieux is recalling VITEK 2 AST-P640 cards because some lots contain insufficient gentamicin, potentially affecting high-level resistance test results.
Beaumont Bio-Med, Inc. is recalling 109 bottles of Muscle & Joint Pain Relief Homeopathic Formula due to CGMP deviations that could result in possible microbial contamination.
Mako Surgical Corporation is recalling 910 units of the Makoplasty RIO Standard System and Ethernet to Fiber Optic Converter due to communication-connection errors.
Degania Silicone is recalling 12,532 Foley catheters with temperature sensors because defective sensors may display lower body temperatures than the patient's actual temperature.
Beaumont Bio-Med is recalling Skin Irritation & Itch Response Homeopathic Formula due to manufacturing deviations that could result in possible microbial contamination.
Siemens is recalling 429 Artis Q Interventional Fluoroscopic X-Ray Systems because a temperature control defect may cause the detector to cool down outside its designed working range.
Beaumont Bio-Med is recalling Colds & Flu Response Homeopathic Formula due to potential microbial contamination from manufacturing deviations.