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.
Thor Motor Coach is recalling 2014-2015 Tuscany XTE motorhomes because the dinette table insert may flip up if sat on, posing a fall risk.
Hitachi Medical Systems America Inc is recalling 173 Oasis Coil Extension Cables used with MRI systems because they may overheat and cause burns.
Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Raymond-Hadley Corp. is recalling Pride of Africa Enriched Farina because the label failed to declare the presence of wheat.
Remel Inc is recalling 1,859 PathoDx Strep Grouping Kits because a reagent may cause weak reactions, potentially leading to failure to identify target species.
B. Braun Interventional Systems is recalling 11 Celsite Implantable Access Port Systems because endotoxin test results were out of specification.
Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Trumpf Medical Systems is recalling 9,287 ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Novacare, LLC is recalling 961 bottles of Glucosamine 750 mg capsules nationwide because the product has inadequate allergen labeling.
Thor Motor Coach is recalling 290 model year 2016 Vegas and Axis recreational vehicles because the HVAC control may lock, preventing windshield defrosting and increasing crash risk.
James G. Cole, Inc. is recalling all ASN brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.
Synthes (USA) Products LLC is recalling 8.5mm Reamer Heads for Flexible Intramedullary Nailing Systems due to the possibility of intraoperative breakage and un-retrieved material fragments.
Niagara Bottling, LLC is recalling multiple brands of natural spring water because source water tested positive for E. coli and total coliform.
Etac Supply Center Ab is recalling 13 units of the Etac Relax wall mounted shower seat due to reports of the wall bracket cracking or breaking.
Trumpf Medical Systems is recalling 9,287 surgical lighting systems because the front joint of the spring arm may break at the monitor interface.
Trumpf Medical Systems is recalling TruLight 3000/5000 surgical lights because the front joint of the spring arm could break at the monitor interface.
Rite Aid is recalling about 13,000 outdoor dining sets because chair arms and legs can bend, causing users to fall and potentially be injured.
Mack is recalling 2011-2016 Granite trucks because an air brake reservoir may have insufficient volume, potentially affecting braking performance and increasing crash risk.
IKEA is recalling PATRULL nightlights because the plastic cover can detach, exposing electrical components and posing a shock hazard.
Tvilum is recalling Stars Mix n'Match Chairs sold at Copenhagen Imports because the legs can break, posing a fall hazard.
Turtle Top is recalling certain 2014-2015 transit buses because the back-up camera system may display reversed images, increasing the risk of a crash.
Forest River is recalling 2013-2014 Starcraft All Star XL and 2013 XLT transit buses because fuel injectors may fail, potentially causing engine stalls and increasing crash risk.
Merck is recalling approximately 276,000 bottles of Temodar and Temozolomide capsules because cracked caps may fail to keep young children from accessing the medication.
Mack Trucks is recalling specific model year 2009-2016 Granite, Titan, and Pinnacle trucks because chassis harness and air lines may not be properly clipped, risking driveline entanglement.
BMW is recalling certain 2012-2015 3-Series vehicles because software may cause front side marker lights to fail, reducing visibility at night.