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.
Hillrom Welch Allyn XScribe cardiac stress testing systems may assign duplicate exam identifiers, potentially causing patient data mismatches in medical record systems.
The Hillrom Welch Allyn Q-Stress Cardiac Stress Testing System may assign duplicate unique identifiers to exam files, potentially causing patient identification mismatches with their cardiac test data.
Hillrom diagnostic cardiology spirometer software may incorrectly assign duplicate identifiers to exam files, risking patient data mismatches. 1,369 units affected worldwide.
DeRoyal is recalling certain lots of children's surgical procedure packs due to reports that the included Stryker smoke evacuation pencil may activate without manual input or remain active after buttons are released.
MyChai Chai Tea Concentrate Original is recalled nationwide. The FDA found pH levels above 4.1 and missing production records.
Certain Hillrom Welch Allyn Vision Express Holter Analysis Systems may assign duplicate identifiers to cardiac exam files, risking mismatch between patient identities and their physiological data.
Smith & Nephew is recalling 21 units of a Tandem Bipolar Hip System component due to an oversized retainer ring in the femoral head assembly. The affected devices were distributed internationally to nine countries.
GE Healthcare's Centricity Universal Viewer Zero Footprint medical imaging software contains a security vulnerability that could allow unauthorized access and patient data manipulation. Approximately 120 units are affected worldwide.
DeRoyal is recalling surgical procedure pack products containing a Stryker SafeAir Smoke Evacuation Pencil that may activate without manual input or remain active after buttons are released. The malfunction poses a risk of injury during surgical procedures.
BMW is recalling certain 2025 X3 30 xDrive vehicles because the right-side head curtain air bag may have been assembled incorrectly, risking delayed or improper deployment in a crash.
Yu Shang Food Inc. is recalling ready-to-eat meat and poultry products due to possible Listeria monocytogenes contamination. Consumers should not eat these items.
Forest River is recalling 2021-2025 Impression fifth wheel travel trailers because the solar charge line, front LED hitch light, and pass-thru light may be wired to incorrect mini breakers, creating a fire risk.
VanCraft is recalling specific 2002-2024 campervans and Rovers because they lack required Occupant and Cargo Carrying Capacity (OCCC) and certification labels.
Vancraft is recalling 2002-2006 Campervans because incorrect seat belt anchor hardware may fail in a crash, increasing injury risk.
Winnebago is recalling 2022 Micro Minnie FLX and Hike travel trailers because solar panel mounting hardware may come loose, creating a road hazard.
Ford is recalling 2024-2025 Escape vehicles with a defective passenger airbag cover that may prevent proper deployment, increasing injury risk and failing to meet federal safety standards.
Forest River and partner brands are recalling approximately 2,783 motorhomes with defective air conditioner soft start devices that may overheat and increase fire risk. Dealers will replace the devices at no charge.
Micro Bird is recalling 2023 CT-Series buses because the ignition interlock may allow the vehicle to start with the rear emergency door locked, increasing injury risk.
Nikola is recalling 2022-2023 Tre BEV vehicles because a resistor may degrade, causing the instrument panel to fail and potentially hide critical safety information.
Hyundai is recalling 34,964 units of the 2024 Santa Fe and Santa Fe Hybrid with faulty switch knobs that may not retract, creating an injury risk.
GM is recalling 2022-2023 Chevrolet Express and GMC Savana vehicles for a transmission software defect that may cause rear wheel lockup and unintended vehicle movement. Dealers will update the software free of charge.
Wolf Appliance is recalling about 44,000 Dual Fuel ranges with infrared griddles due to a short-circuit hazard. Liquid spillage can unexpectedly activate the griddle, posing burn and fire risks. No injuries have been reported.
Dreamgro Lullaby mermaid travel soothers are recalled because a gold-colored soft star can detach, posing a choking hazard to infants. No injuries have been reported, but one detachment incident was confirmed.
Kyte Baby is recalling about 20,500 Slumber Suits sold from November 2022 to March 2024 because they violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. No injuries have been reported.
Guava Roam strollers are recalled because the brakes can fail to engage or unexpectedly disengage, posing fall and injury hazards to children. No injuries have been reported.