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.
New Seasons Market LLC is recalling Blueberry Buckwheat Muffins because the packaging fails to declare egg as an ingredient.
Siemens is recalling 14 Artis zee floor systems because the display may fail to show images after power save mode, potentially requiring treatment cancellation.
Siemens is recalling 73 Artis zee ceiling units because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Philips is recalling 28 Ingenuity Core128 MRI systems because a production defect in the X-Ray Tube allows oil leakage, posing a risk to patients and users.
Siemens is recalling Artis Q.zen floor units because the display may fail to show images after power save mode, potentially requiring procedure cancellation or patient transfer.
Siemens is recalling four Artis Q.zeego X-ray systems because the display may remain black after power save mode, preventing normal operation and requiring procedure cancellation or patient transfer.
St Jude Medical is releasing new firmware for Merlin PCS programmers to strengthen security against unauthorized access to cardiac devices.
Safe N Simple is recalling No-Sting Skin Barrier Film wipes due to confirmed bacterial contamination that poses a risk of infection.
Siemens is recalling five Artis Q biplanes because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.
Forest River and Coachmen are recalling specific RV models because liquid leaks into the driver's power window switch, causing corrosion and increasing the risk of a fire.
Lippert Components is recalling Solera Smart Arm Awnings because water intrusion may cause them to deploy while driving, increasing crash risk.
BRP is recalling about 13,300 2018 Can-Am Outlander and Renegade ATVs because fuel can spray from the tank when opening the gas cap, posing a fire hazard.
Helmets R Us is recalling about 9,700 Rollerblade helmets sold to schools because they fail to meet federal safety standards, posing a risk of head injury.
Suzuki is recalling 2018 DR-Z400S and DR-Z400SM motorcycles because resin may prevent the rear brake light from illuminating, increasing crash risk.
General Motors is recalling 2016-2018 Cadillac CT6 vehicles because excess adhesive on child seat anchorage bars may interfere with proper installation, increasing injury risk.
Newmar is recalling 2018 motorhomes because slide-out rooms may move unexpectedly when the ignition is off, increasing the risk of injury.
Zimmer Biomet is recalling 2,396 trauma guide wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
Zimmer Biomet is recalling 26 units of Ball Tip Guide Wires because packaging defects may allow sterile barrier breaches, posing a risk of infection.
World Variety Produce Inc. is recalling Melissa's Spicy Edamame because the included flavoring packet contains oyster sauce, an undeclared allergen.
Zimmer Biomet is recalling trauma guide wires because packaging defects may allow sterile barrier breaches, creating a risk of infection.
Agro Sevilla USA is recalling H-E-B Ode to Olives, Sliced Salad Olives, because two jars were found to contain pieces of glass. No injuries have been reported.
CryoLife, Inc. is recalling one unit of Cryopatch SG Pulmonary Human Cardiac Branch because final autopsy and toxicology reports indicated the presence of morphine in the donor's urine.
TriMed Inc. is recalling 323 Nitinol staples because evidence of required quarterly sterilization dose audits could not be found, posing a potential infection risk.
Synthes (USA) Products LLC is recalling 7 units of a combined cannulated screw set because the included gauges measure screws 5.41mm shorter than actual length.
Vascular Solutions, Inc. is recalling specific lots of Drainer Centesis Catheters because the supplier reported a potential for unsafe levels of bacterial endotoxins.