Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Daimler Trucks North America is recalling 2018-2019 Thomas Built Buses Saf-T-Liner C2 transit buses because a battery cable may rub against a bracket, increasing the risk of a fire.
Wild & Wolf is recalling Petit Collage wooden toy xylophones because the beater stick ball can detach, posing a choking risk to young children.
General Motors is recalling 2018 Chevrolet Equinox vehicles because the front door window glass may not be properly tempered, increasing injury risk if broken.
Polaris is recalling about 10,900 Ranger XP recreational off-highway vehicles because the center seat belt bracket can separate from the frame, posing an injury hazard to riders.
Kumho is recalling specific Solus KH16 tires because the belts may separate under severe conditions, increasing the risk of a crash.
Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses school buses because a wall mounting bracket may crack, increasing injury risk in a crash.
Base Brands is recalling Reduce Hydro Pro water bottles because the pink paint on the bear design exceeds federal lead paint standards.
Arrow International is recalling specific lots of Arrowg+ard Blue MAC Two-Lumen Central Venous Access Kits because the catheters may not be completely sealed, compromising sterility.
Precise Food Ingredients is recalling 896 pounds of Roast Beef Gravy Seasoning due to potential Salmonella contamination. The product was distributed in Texas.
Philips is recalling 975 IntelliVue X3 Patient Monitors because they may display incorrect blood pressure values or become inoperable due to touch interface issues.
Arrow International is recalling specific lots of MAC Two-Lumen Central Venous Access Kits because the seals may be incomplete, preventing a guarantee of sterility.
Poppies International is recalling three brands of frozen Belgian mini eclairs because they may be contaminated with Listeria monocytogenes.
Arrow International Inc is recalling specific lots of arterial catheterization kits because the products may not be completely sealed, meaning sterility cannot be guaranteed.
Mindray is recalling specific lots of M-30D diluent used with BC-3200 and BC-3600 analyzers because they may cause the system to produce an elevated platelet background count.
Arrow International is recalling specific lots of Multi-Lumen Hemodialysis Catheterization Kits because the seals may be incomplete, preventing a guarantee of product sterility.
Arrow International is recalling specific lots of ARROWg+ard Blue Central Venous Catheter (CVC) kits because the products may not be completely sealed, meaning sterility cannot be guaranteed.
ICU Medical is recalling 250 pouches of 7-inch intravascular administration sets because they were manufactured with an incorrect spin collar.
Arrow International Inc is recalling specific lots of cardiovascular catheters because the products may not be completely sealed, meaning sterility cannot be guaranteed.
Arrow International is recalling specific lots of two-lumen PICC kits because the catheters may not be completely sealed, potentially compromising sterility.
Hamilton Medical AG is recalling 739 Hamilton-C3 Ventilator Units worldwide because the battery fuel gauge may inaccurately indicate a higher charge than available.
Teleflex Medical Europe Ltd is recalling 107,962 latex rebreathing bags because they lack the required warning that the product contains natural rubber latex, which may cause allergic reactions.
Arrow International is recalling specific lots of central venous catheter kits because they may not be completely sealed, preventing a guarantee of sterility.
Lifeline Systems is recalling Model FD100 HomeSafe AutoAlert Pendants because a programming error disables the fall detection feature.
C.R. Bard is recalling specific lots of Bard Adult/Pediatric Feeding Tubes because the tubing and ENFit connector may not be fused effectively.
Newmar is recalling specific 2013-2017 motorhomes because low beam headlights turn off when high beams are activated, reducing driver visibility.