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.
Rossmonster is recalling 2026 Baja, Skye, and Havn motorcoaches because a rooftop ventilation fan component may overheat and cause a fire.
Modine is recalling Airedale ventilation fans in specific school heat pumps because water exposure can cause short circuits and fires. No injuries have been reported.
CCM Hockey is recalling FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories because they can crack upon impact, posing a risk of laceration or impact injury.
CPSC recalls Koorlian mattresses sold on Amazon due to fire risks from violating mandatory flammability standards. Consumers should stop using them and contact the manufacturer for a free cover.
Marathon Industries is recalling one 2025 Ford F-650 SD because deck pins may break, causing the liftgate platform to fall and increasing injury risk.
Britax is recalling specific infant car seats because a screw in the carrying handle may come loose, causing the handle to partially detach and increasing the risk of a child falling.
Victory Medical Center Pharmacy is recalling 91 vials of Glutathione (MDV) 200 mg/mL due to bacterial endotoxin contamination.
Liebel-Flarsheim is recalling 3,486 vials of Optiray Injection due to the presence of particulate matter, including plastic, stainless steel, and glass.
Apollo Care, LLC is recalling 250 vials of Semaglutide 2.5mg due to the presence of nylon and silk particulate matter.
Apollo Care, LLC is recalling specific lots of Semaglutide 6.75mg vials because they contain nylon and silk-type particulate matter.
Prestige Brands Holdings is recalling Clear Eyes Maximum Itchy Eye Relief eye drops due to a lack of assurance of sterility and potential contamination.
Apollo Care, LLC is recalling 56,918 vials of Semaglutide 12.5mg due to the presence of nylon and silk particulate matter.
Shoolin Pharma Chem LLP is recalling Tadalafil USP 1.00 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.
Apollo Care, LLC is recalling specific lots of Semaglutide 20mg vials because they contain nylon and silk-type particulate matter.
Apollo Care is recalling 250 vials of Semaglutide 7.5mg due to the presence of nylon and silk-type particulate matter.
Baxter Healthcare is recalling 19,032 bags of Cefazolin Injection due to the presence of particulate matter. The affected product is distributed nationwide in the US.
Covidien is recalling Dermalon 4-0 sutures because sterile barrier packaging may be perforated or torn, risking biocontamination and infection.
Apollo Care, LLC is recalling 4,748 vials of Semaglutide 0.9mg due to the presence of nylon and silk particulate matter.
Apollo Care, LLC is recalling 250 vials of Semaglutide 5mg due to the presence of nylon and silk-type particulate matter.
FDA is recalling Surgipro II sutures due to potential sterile packaging defects that could cause biocontamination and infection.
Apollo Care, LLC is recalling specific lots of Semaglutide 2.25mg vials because they contain nylon and silk-type particulate matter.
Apollo Care, LLC is recalling 9,762 vials of Semaglutide 4.5mg due to the presence of nylon and silk-type particulate matter.
Erbe USA Inc is recalling ERBECRYO 2 Cryosurgical Units because a strong pull on the high-pressure transfer hose may cause the cryoprobe to rupture.
Apollo Care, LLC is recalling 500 vials of Semaglutide 10mg due to the presence of nylon and silk-type particulate matter.
FDA is recalling V-Loc 180 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that could lead to biocontamination.