State
72,919 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 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Head ski boots with fluorescent yellow components from model years 2016 through 2022 are recalled because those materials can deteriorate and break, posing a risk of injury from a fall.
Breez 2-in-1 Smart Bedroom Fan and White Noise Machines are recalled because the internal power connector can corrode and cause the fan to overheat, posing a fire risk.
The Member's Mark 7-foot Pre-Lit Twinkling Buck is recalled because the current limiting resistor can overheat if the wires are connected incorrectly, posing a burn hazard. About 2,460 units are affected.
Muscccm pool drain covers are recalled because they violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act, posing entrapment and drowning hazards.
Besslly Halloween Pumpkin Carving Kits are recalled because children can easily access the button cell batteries in the included tea lights, posing an ingestion hazard. About 650 units are affected.
Happiness Light LED lights are recalled because their lithium coin batteries can be accessed easily by children, posing an ingestion hazard. About 2,800 units are affected.
Iron-containing dietary supplements from eleven brands are recalled because their packaging is not child-resistant as required by the Poison Prevention Packaging Act. About 356,140 units are affected.
Yeeluzan pool drain covers are recalled because they violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act, posing entrapment and drowning hazards.
Male-to-male extension cords sold on Walmart.com are recalled because their exposed prongs can become energized when one end is plugged into a generator, posing an electrocution risk.
ShymeryDirect LED lights are recalled because their lithium coin batteries can be accessed easily by children, posing an ingestion hazard. About 295 units are affected.
One lot of Magnesium Sulfate in Water for Injection is being recalled after a foil pouch labeled as magnesium sulfate was found to contain an IV bag of tranexamic acid.
Philips Respironics is recalling the Trilogy Evo ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy Evo Universal ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy EV300 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips Respironics is recalling the Trilogy Evo O2 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Philips is recalling the Allura Xper FD20 Biplane because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Burlington Medical is recalling wrap aprons made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
Medtronic is recalling Paradigm REAL-Time insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Intuitive Surgical is recalling da Vinci S and Si Permanent Cautery Hook Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Burlington Medical is recalling kilts made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
One Paradise Ultrasound Renal Denervation catheter was distributed although it was a nonconforming product that should have been scrapped and not used in humans.
Burlington Medical is recalling thyroid shields over the potential for attenuation degradation over time, which decreases the product's usable lifespan. 41,962 units are affected.
GoodSense Eye Drops Original Formula, containing tetrahydrozoline hydrochloride, are being recalled for lack of assurance of sterility.
Medline is recalling ENFit G-tube connectors because they were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices.
Medline is recalling six bronchoscopy and thoracic kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.