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.
TheKiddoSpace is recalling its Peg Dolls in Cups Toys because the small peg dolls pose a choking hazard to children under three years old.
Honda is recalling certain 2024 Acura ZDX and Prologue vehicles because a software error may cause the instrument panel display to fail and the rearview camera to show a blank screen in reverse.
TheKiddoSpace is recalling approximately 650 LED soccer hover balls because the battery surface temperature can exceed safety limits, posing a burn risk.
SumDirect LED Mini Lights are recalled because the button cell batteries can be easily accessed by children, posing an ingestion hazard. No injuries have been reported.
Andersen Windows is recalling about 91,000 window opening control devices sold as kits or installed on 100 Series casement windows because they can break or detach after impact, posing fall and serious injury hazards. No injuries have been reported.
About 81,800 Babysense Max View baby monitors are recalled because the display unit can overheat and spark while charging, creating a fire hazard. Hisense has received 11 incident reports with no injuries reported.
About 150 Bicystar high chairs (model TB-HC6900) sold on Amazon are recalled because they lack the required crotch restraint and can trap a child's head, creating fall and entrapment hazards. No injuries have been reported.
BMW is recalling one 2026 S 1000 RR motorcycle because the turn signal reset button can be unintentionally activated, causing the turn signal to fail.
PQL recalls about 186,520 high bay linear LED light fixtures because degrading retaining pins can cause the LED board to come loose and spark a fire. One fire has been reported with no injuries.
TheKiddoSpace is recalling about 140 children's story books because felt parts can detach and pose a choking hazard. No injuries have been reported.
Joyreal Busy Board children's toys are recalled due to choking and laceration hazards from a detachable small mirror with sharp edges. No injuries have been reported.
Evajoy 48-inch and taller above-ground pools are recalled due to a drowning hazard. The compression strap around pool legs can create a foothold allowing child access.
TheKiddoSpace is recalling its Children's Sensory Swing because the flexible fabric can form loops that pose a risk of serious injury or death from strangulation.
TheKiddoSpace is recalling approximately 300 Children's Christmas Tree Toy Play Sets because the zipper pulls contain lead levels that exceed federal limits.
Todson is recalling about 40,245 Concord 360 Degree Rechargeable Light-Up Bike Helmets because they fail to meet safety standards, posing a risk of serious head injury or death.
Magnetic chess games sold on Amazon by Kaiwenshangpin are recalled because loose magnets inside can be swallowed by children, potentially causing intestinal damage or death. No injuries have been reported.
TheKiddoSpace is recalling about 19,700 children's handwriting practice kits because the pens contain lead levels that violate the federal lead content ban. No injuries have been reported.
TheKiddoSpace is recalling approximately 4,000 children's flashcard talking toys due to lead and phthalate levels that exceed federal limits and a failure to meet battery safety standards.
TheKiddoSpace is recalling about 4,300 reusable water balloons because the cord lock on the storage bag contains a regulated phthalate that violates the federal phthalate ban. No injuries have been reported.
Immunotech A.S. is recalling 160 Estrone RIA kits (REF: DSL8700) that may rarely give falsely high patient results, which could cause temporary injury with remote probability.
Medline Industries, LP is recalling certain Medline Convenience Kits (Dental Pack, Model DYNDA3003) because equipment calibration issues may have impacted the sterility of the products.
Medline Industries is recalling cardiac surgical convenience kits due to sterilization equipment calibration issues that could affect device sterility assurance levels.
Medline is recalling 2,740 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Pure Solutions, Inc. is recalling Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset because the labels do not declare milk as an allergen.
Medline is recalling 23,238 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.