State
72,816 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 72,816 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
YERYORK pressure washers are recalled because they lack a ground-fault circuit-interrupter, posing a risk of shock or electrocution.
AudioLineOut is recalling Studio Six Headphone Amplifiers because they pose a risk of serious injury or death from electrocution when used with aftermarket metal base tubes.
Steelite electric pressure washers are recalled because they lack a ground-fault circuit-interrupter and adequate power cord, posing a risk of serious injury or death.
Altec is recalling 2021-2023 Service Body vehicles because water leaks into strobe lights, causing electrical short-circuits that increase fire risk.
Kmaier recalls infant walkers that violate safety standards by failing to stop at step edges, posing a risk of serious injury or death.
HABA USA is recalling Rainbow Rattle Grasping and Teething Toys because a glued knot can untie, exposing small parts that pose choking and ingestion risks to young children.
Excel Industries is recalling about 1,800 accessory LED light kits for Hustler and BigDog ride-on mowers because the light bars can overheat or produce flames.
Diamond Wipes International is recalling MD Wipe Outz Numbing Tattoo Wipes because the packaging is not child-resistant, posing a risk of serious injury or death from child poisoning.
Little Loves & Co. is recalling youth clothing sets with drawstrings due to an entrapment hazard that could cause serious injury or death to children.
Coast Citrus Distributors is recalling bulk jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed to wholesale distributors and has not been sold at retail.
American Regent, Inc. is recalling Papaverine Hydrochloride Injection due to the presence of glass and/or paraformaldehyde particulate matter.
Fresenius Kabi is recalling 625,500 Morphine Sulfate syringes because some were mislabeled and contained Dilaudid instead.
American Regent, Inc. is recalling Nitroglycerin injection vials due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling Acetylcysteine Solution USP due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling specific lots of Cyanocobalamin injections due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling Selenious Acid Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling 43,460 vials of Nicardipine Hydrochloride Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
Tobii Dynavox is recalling TD Navio Midi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.
American Regent, Inc. is recalling Atropine Sulfate injection vials because they contain particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling Cyanocobalamin injections because they contain particulate matter, including hair, glass, and paraformaldehyde.
Siemens is recalling 20 units of the Syva EMIT 2000 Quinidine Assay due to precision issues that may cause inaccurate test results.
Tobii Dynavox is recalling TD Navio Maxi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.
Shilpa Medicare is recalling 18,434 vials of PEMRYDI RTU (pemetrexed injection) due to reports of green to dark green discoloration in the solution.
American Regent is recalling 323,000 vials of Tralement (trace elements injection 4) due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
Regeneron is recalling 21,353 vials of Libtayo (cemiplimab-rwlc) injection nationwide due to a lack of assurance of sterility.