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.
Heartland Coca-Cola Bottling Company is recalling 766,271 cases of 12 oz Vanilla Coca-Cola cans due to sharp edges that may cause cuts.
Heartland Coca-Cola Bottling Company is recalling Diet Coke Caffeine Free cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.
Cameron Company is recalling Playtime Pals Pop-Up Hideaway Hut children's tents because the fiberglass support rods can break and splinter, posing a laceration hazard.
Heartland Coca-Cola Bottling Company is recalling 766,271 cases of Diet Coke cans because sharp edges were observed, posing a risk of mouth cuts.
MAAX Spas is recalling about 550 hot tubs and swim spas in the U.S. because the internal UV generator can ignite, posing a fire hazard.
Honda is recalling 2014-2016 Odyssey vehicles because the second row left outboard seatback may fail to lock, increasing injury risk in a crash.
Helvetia Sports is recalling SwissStop EXOTherm cycling disc brake pads because they can separate from the backplate, posing a fall hazard to users.
Hyundai is recalling 2016-2018 Sonata Plug-In Hybrids because a voltage protection device may activate inadvertently, causing loss of power and increasing crash risk.
Forest River is recalling 2018 Stealth Evo recreational trailers because the federal placard lists incorrect tire sizes. This error could lead owners to install wrong replacement tires, increasing crash risk.
Ferrari is recalling 2016 488 GTB and 488 Spider vehicles because a software error may prevent drivers from receiving warnings about critically worn brake discs.
Heartland Catfish Company is recalling approximately 69,016 pounds of fresh and frozen catfish products that may be adulterated with leucomalachite green, a residue of public health concern.
Supreme Corporation is recalling 2003-2018 trucks equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks during a fire.
Kia is recalling 2017-2018 Optima hybrid vehicles because a voltage protection device may activate inadvertently, causing a loss of power in EV mode and increasing crash risk.
BDA is recalling Golden State Warriors Menorahs because the glue holding the candleholders can melt, causing lit candles to fall and posing fire and burn risks.
American Technology Components is recalling specific 7-Way Wiring Harnesses used for aftermarket truck cap installations because the wiring may overheat, increasing the risk of a fire.
Siemens Medical Solutions is recalling 510 foot switch accessories for Artis zee and Artis zeego x-ray systems because they may fail to release radiation.
Elekta Limited is recalling Agility with Integrity R3.2 software due to a potential for positional errors following automatic table movement.
Daimler Trucks North America is recalling 2007-2018 Thomas Built Buses Minotour vehicles because the wheelchair lift may operate while the bus is in motion.
Alto Development Corp is recalling surgical punches because packaging damage during transport may have compromised sterility.
3M is recalling 120,000 Surgical Clipper Professional 9681 units worldwide due to lithium-ion battery degradation risks, including excessive heat and potential venting.
Zimmer Biomet is recalling 337 Phoenix Antegrade Femoral Nail Connecting Bolts because the bolt may fracture during insertion of the femoral nail.
Zevex Incorporated is recalling Moog Curlin Infusion Administration Sets due to particulate matter found on the spike. The recall covers 56,244 cases distributed nationwide and internationally.
DePuy Mitek is recalling FMS Gravity Tube Sets because they may leak at the bulb and tube connection during arthroscopic procedures.
Stryker is recalling 1,162 Berchtold Chromophare surgical lights because missing parts could cause the equipment to fall.
Siemens Medical Solutions is recalling Artis Zee and Zeego devices due to a potential for liquid entry.