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.
Nissan is recalling 2013 Armada and Titan vehicles because a brake master cylinder defect may reduce front brake pressure, increasing the risk of a crash.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Folate test kits due to calibration failures and significant negative shifts in quality control and patient results.
Lumenis is recalling three Vision One Laser Systems due to a potential for unintended laser exposure to the user.
Beacon Hill Medical Pharmacy is recalling Sermorelin Acetate 10 mg injectable because FDA inspectional findings raised concerns about sterility assurance and quality control.
B. Braun Medical is recalling 900 Outlook Safety Infusion System Burette Sets because one injection site and valve were assembled upside down.
Beacon Hill Medical Pharmacy is recalling Methylcobalamin injections because FDA inspections found quality control issues that impacted sterility assurance.
Craftsmen is recalling 2006-2013 custom vehicles with Fastec door locks that may jam, potentially trapping occupants inside the vehicle.
The Children's Place is recalling about 38,000 footed pajamas in the U.S. because they fail federal flammability standards, posing a burn hazard to children.
Chalet RV is recalling 2006-2013 travel trailers and truck campers because a door lock defect could jam the deadbolt, trapping occupants inside.
Augusta RV is recalling 189 FLEX recreational vehicles because a door lock defect may jam the deadbolt, potentially trapping occupants inside the vehicle.
Cowtown Sleepers is recalling 2008-2013 truck sleepers because a door lock defect may jam the deadbolt, potentially trapping occupants inside the vehicle.
Hart Trailer LLC is recalling 2006-2013 Medallion, Ultimate, and Cargo horse trailers because a door lock defect may jam, trapping occupants inside.
PROLine is recalling 2006-2013 travel trailers with Fastec door locks that may jam, potentially trapping occupants inside the vehicle.
Arising Industries is recalling 2008-2013 cargo trailers because a door lock defect may jam the deadbolt, trapping occupants inside.
Coose Trailer is recalling 2006-2013 travel trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside.
Horton Vans is recalling 2006-2013 cargo trailers with Fastec door locks that may jam, potentially trapping occupants inside.
Pleasant Valley is recalling 2006-2013 travel trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside the vehicle.
Adventurer LP is recalling 2009-2012 truck campers because a door lock defect may jam the deadbolt, trapping occupants inside the vehicle.
Genie is recalling 3,889 TZ-34 aerial work platform trailers because the outrigger assembly may not stay stowed during transport, increasing crash risk.
Lakota is recalling two 2007 travel trailer models because a door lock defect may jam the deadbolt, potentially trapping occupants inside the vehicle.
Dolan Designs is recalling about 8,000 ceiling-mounted light fixtures because degraded wire insulation can expose charged wires, creating fire and electric shock risks.
Cimarron Trailers is recalling 2006-2012 livestock trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside.
Champion Bus is recalling 598 buses from 2009-2011 because voltage spikes may damage door header circuit boards, increasing the risk of a fire.
Genzyme is recalling LeGoo Endovascular Occlusion Gel because the product contains particulates (fibers). The recall covers 660 units distributed worldwide.
Genzyme Corporation is recalling LeGoo Endovascular Occlusion Gel because the product contains particulates (fibers). The recall affects 220 units distributed worldwide.