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.
Ricky Joy is recalling over 2.3 million Sour Crush Rolling Liquid Candy bottles because the rolling ball can detach, posing a choking hazard.
FJTJBSI is recalling about 9,000 six-drawer dressers sold on Amazon because they violate safety standards and pose tip-over and entrapment risks to children.
Forest River is recalling 2019-2022 Lone Star Vans because cracks in the microprocessor may prevent the rearview camera from displaying properly, increasing crash risk.
Ford is recalling 2026 F-150 vehicles because stabilizer rod fasteners may not be tightened properly, which can cause the rod to shift and increase crash risk.
Philips is recalling Brilliance CT systems due to an unintended radiation issue that could affect equipment performance.
AVID Medical is recalling specific lots of Halyard medical convenience kits containing Ritmed Neurological Sponges due to potential endotoxin level variability.
Prince Bakery Inc is recalling 150 units of Prince Italian Bread in New York because sesame is not declared in the ingredient statement.
Ford is recalling 2026 Bronco vehicles because a metal burr on the side curtain air bag bracket may tear the bag during deployment, increasing injury risk.
Baxter Healthcare is voluntarily recalling specific lots of Vancomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Medline is recalling 3,752 Labor CDS and Vag Delivery Admission Bags due to packaging wrinkles that may compromise sterility, risking microbial contamination.
Baxter Healthcare is recalling four Novum IQ Syringe Pump loaner units due to a software issue that may occur during multi-syringe infusions.
Medline is recalling blood culture kits containing BD ChloraPrep applicators due to potential packaging seal defects that could lead to infection.
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could lead to infection.
Medline is recalling blood culture kits containing BD ChloraPrep applicators with open or incomplete seals. The defect may allow contamination, posing a risk of infection.
Prince Bakery Inc is recalling 150 units of Pan De Manteca in New York because milk is not declared in the Contains statement.
Medline is recalling specific lots of convenience kits containing BD ChloraPrep applicators due to potential packaging seal defects that could allow contamination.
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators because packaging seals may be open or incomplete, posing a risk of infection.
Philips is recalling Brilliance CT 64 systems due to an unintended radiation issue that could affect equipment performance.
Medline is recalling 176 colorectal convenience kits due to potential packaging defects that may compromise sterility, posing a risk of microbial contamination.
AVID Medical, Inc. is recalling specific lots of Ritmed Neurological Sponges Non-Sterile due to potential unexpected variability in endotoxin levels.
Philips is recalling IQon Spectral CT systems due to an unintended radiation issue that could affect equipment performance.
Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Medline is recalling Ortho Aspiration Kits containing BD ChloraPrep applicators due to packaging seal defects that may allow contamination.
Medline is recalling 17,750 IVS Blood Culture Kits nationwide due to potential packaging defects that may compromise sterility.
Baxter Healthcare is recalling 14,601 Novum IQ Syringe Pumps due to a software issue that may occur during multi-syringe infusions.