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.
Walker Edison is recalling about 24,000 drawer chests because they are unstable if not anchored, posing tip-over and entrapment hazards to children.
CME America LLC is recalling 27 BodyGuard Wall Chargers because they may not properly charge the infusion pump battery.
Merge Healthcare is recalling 47 units of Merge LIS software because a defect causes unrelated medications to appear on patient reports.
RTI Surgical is recalling 420 units of Streamline MIS Navigation System Taps because they have experienced binding with other devices.
Foreign Tire Sales, Inc. is recalling 138 Otani OH-306 commercial truck tires with DOT code 0320 because a manufacturing defect may cause the tread to crack.
USDA FSIS issued a public health alert for Kwik Trip spaghetti and meatballs in marinara sauce due to possible metal contamination. Consumers should not eat these products.
Smith & Nephew is recalling 143 units of 5.5MM Arthrogarde Hip Access Cannulas because the J Lock feature was manufactured incorrectly, preventing proper locking into irrigation extenders or arthroscopes.
Target is recalling approximately 122,500 Cat & Jack toddler boots because the toggle can detach, posing a choking hazard to children.
W.L. Gore is recalling GORE TAG stent grafts because the delivery catheter could not be withdrawn after implantation.
GE Healthcare is recalling 64 CT scanners worldwide because incorrect settings may cause smudge artifacts that could be mistaken for pathology.
Intuitive Surgical is recalling one da Vinci Xi Endoscope Controller because improper calibration may cause the endoscope tip to reach higher temperatures, potentially leading to thermal tissue injury.
Thor Motor Coach is recalling 2010-2011 Four Winds Montecito motorhomes because a transfer switch may fail due to heat, increasing fire risk.
Philips is recalling 8,942 sterilizable defibrillator paddles because standard checks may miss a specific failure mode. An updated test procedure is available to detect the issue.
Transcraft is recalling 2016-2021 Platform trailers because adjustable wheel stops may detach, increasing the risk of crash or injury.
YETI is recalling Rambler 20 oz Travel Mugs with Stronghold Lids because the magnetic slider can eject, causing hot liquid to spill and posing burn risks.
Hu Products is recalling chocolate-covered cashews that may contain undeclared almonds. Consumers with tree nut allergies should not consume the product.
Mercedes-Benz is recalling certain 2020-2021 GLE models because the middle seat belt buckle may fall into a gap, rendering it inoperable and leaving occupants unrestrained.
Certain 2020-2021 Keystone Cougar trailers with solar packages have incorrectly wired inverters that may energize shore power connections, creating a risk of electrical shock.
Mercedes-Benz is recalling certain 2019-2021 vehicles because the front passenger seat may be missing a mechanical adjustment limit stop. The seat could move outside the safe range relative to the airbag, increasing injury risk in a crash.
Jayco, Inc. is recalling certain 2020-2021 motorhomes due to engine covers with insufficient heat insulation. This may cause excessive interior surface temperatures that increase the risk of injury to occupants.
Gorilla Commerce is recalling about 1,600 heavy duty oven liners sold online because they may block oven vents, creating a risk of carbon monoxide poisoning.
Serena & Lily is recalling Nash Convertible Cribs because a leg can partially detach from the headboard or footboard, posing an injury hazard.
ICU Medical is recalling specific lots of NanoClave intravascular administration sets because a manufacturing defect may prevent a proper seal with the spike.
ICU Medical is recalling specific lots of 7-inch smallbore extension sets because a manufacturing defect may prevent the NanoClave from sealing properly.
ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.