State
72,940 recalls have nationwide distribution and so reach Puerto Rico. 3,090 additional recalls listed Puerto Rico specifically in their distribution scope.
Of the 3,090 recalls naming Puerto Rico we have scored against our rubric, 366 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 625 (20%) are Severe.
Which agencies issued them
These figures cover only the 3,090 recalls whose distribution notice names Puerto Rico specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Philips North America is recalling the IntelliVue Multi Measurement Server X2 over a potential issue where the monitors did not alarm.
Paragon 28 is recalling 20 Phantom Fibula Nails because out of specification thread depths may prevent the implant from mating with its mounting bolt, potentially requiring surgery to be aborted.
Philips North America is recalling the IntelliVue Patient Monitor MX100 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX600 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP60 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP80 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX750 over a potential issue where the monitors did not alarm.
Medtronic is recalling 6,591 Aurora EV-ICD and Clinical EV-ICD single chamber extravascular defibrillators over the potential for delayed time to high-voltage therapy in a rare sequence of events.
Motor Coach Industries is recalling various transit bus models because the front door lower curb view glazing material is incorrect, which may reduce driver visibility and increase crash risk.
Great Lakes Cheese is recalling 235,789 cases of low-moisture part-skim mozzarella shredded cheese, sold under 26 brands, over potential metal fragments from a supplier raw material.
Illumina is recalling 11,916 NextSeq 550Dx reagent kits because flow cell gaskets have a quality issue that may cause leaks during runs, including possible toxic substance exposure to the user.
Costco is recalling 142,532 retail units of Kirkland Signature Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Water Pure is recalling 17,612 bottles of My Bladder dietary supplement because the product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303.
Costco is recalling 612 retail units of Kirkland Signature Chicken Sandwich with Caesar Salad because the 3 oz sealed packet of Caesar dressing may contain plastic material.
Philips North America is recalling the IntelliVue MP40 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX550 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP20 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX700 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP90 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP30 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX800 over a potential issue where the monitors did not alarm.
Get Tested International AB is recalling 1 unit of its Environmental Pollutants Profile Test because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 3 units of its Food Sensitivity Test Small because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 1 unit of its GI Microbiome Profile Small because the product was distributed without premarket approval or clearance.
Get Tested International AB is recalling 80 units of its Cholesterol Test because the product was distributed without premarket approval or clearance.