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.
Harmony Juvenile Products is recalling Big Boost Deluxe booster seats because the seat belt may apply excessive force to a child's chest in a crash.
Lamborghini is recalling 11 2017 Centenario vehicles because an incorrect weight limit on the certification label may allow the vehicle to be overloaded.
KZRV is recalling 2019 Connect recreational trailers because an incorrect circuit breaker may increase the risk of a fire. Dealers will replace the part free of charge.
Schneider Electric is recalling Square D safety switches because power may remain on when the handle is in the OFF position, posing an electrical shock hazard.
Jo-Ann Stores is recalling battery-operated LED light sets because the glass jars can break during normal use, posing a laceration hazard.
Gulf Stream is recalling 2016-2018 Conquest and B Touring Cruiser motorhomes because they lack required intermediate side marker lights, increasing crash risk.
Nissan is recalling 2016-2018 Titan and Titan XD trucks because missing labels may allow owners to overload the vehicles, increasing crash risk.
Forest River is recalling 2017-2019 Crossfit coaches because incorrect weight placards may lead to vehicle overloading and increased crash risk.
Group Rossignol is recalling LOOK Pivot ski bindings because the heel piece can loosen, posing a fall hazard to skiers.
Forest River is recalling 2018-2019 FR3 and Georgetown recreational vehicles because the entry door latch may not engage fully, allowing the door to open unexpectedly while moving.
General Motors is recalling 2018 Buick Regal vehicles because rear seat belts may be improperly routed, potentially failing to restrain passengers in a crash.
Forest River is recalling 2018 Salem recreational trailers because the federal placards list incorrect tire pressure, which may lead to under-inflation and increased crash risk.
L.L.Bean is recalling Allagash fixed blade hunting knives because the blade can cut through the leather sheath, posing a laceration hazard.
Kaltic Food Packaging is recalling Frank & Tony's New York Style Red Onion Sauce because it contains undeclared fish (anchovy).
GE Healthcare is recalling 1,742 units of the Monica Novii Wireless Patch System because incorrectly reconnected cables may cause fetal and maternal heart rate signals to be displayed swapped.
Fresenius Medical Care is recalling 127 K2 Hemodialysis Machines because a software defect may allow the ultrafiltration pump to run at unsafe rates during SLED treatments.
Baxter Healthcare is recalling 3,440 Prismaflex Control Units worldwide due to reports of operators failing to follow safe unloading instructions and software errors in specific versions.
C.R. Bard is recalling specific lots of HydroSil Gripper Intermittent Catheters because some units were found caught in the sterile barrier seal or cut.
Supreme Bakery LLC is recalling 50 loaves of Moskovski Batton bread in Massachusetts due to undeclared milk and soy ingredients.
DePuy Spine is recalling specific lots of the Confidence Plus Kit Spinal Cement System because they may contain incorrect amounts of contrast medium, making the product difficult or impossible to visualize on x-ray.
C.R. Bard is recalling Magic 3 Intermittent Catheters because some units were caught in the sterile barrier seal or cut.
Seiler Instruments is recalling Alpha Air 6 ENT Microscopes because they may tip over if attachments are extended and the device is moved improperly.
GE Healthcare is recalling 355 Monica IF24 Interface Systems because incorrectly reconnected cables can cause fetal and maternal heart rate signals to be displayed incorrectly.
Magellan Diagnostics is recalling 79 LeadCare Plus Blood Lead Analyzers because incorrect battery placement may cause overheating and potential finger burns.
Magellan Diagnostics is recalling LeadCare II Blood Lead Analyzers because incorrect battery placement may cause overheating and potential finger burns.