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.
Coastal Meds, LLC. is recalling 745 vials of Cyanocobalamin Injectable due to the presence of unknown particulate matter.
Maharaja Food Importers is recalling frozen MMRF Ela Ada Jaggery because the label lists ghee but fails to declare milk, a major allergen.
Stryker is recalling T4 Zipper Toga sterile personal protection garments because material layers may separate, posing a risk of exposure to contaminants.
Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires due to potential failure of the sterile packaging seal.
Life Technologies is recalling 30 units of the Oncomine Dx Target Test because a lower RNA concentration could cause false negative results for ROS1 fusion, potentially affecting patient treatment.
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.
Carter's is recalling 3-piece penguin cardigan sets because the toggle button can detach, posing a choking hazard to young children.
Traditional Medicinals is recalling specific lots of organic EveryDay Detox Lemon tea because raw material tested positive for Salmonella.
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, creating a potential risk of exposure to contaminants.
Coastal Meds, LLC. is recalling LIPO-B Injectable-30 mL vials due to the presence of unknown particulate matter.
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.
Integra LifeSciences is recalling 1,619 humeral stem trials for the Titan Modular Shoulder System because they may break during surgery.
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, creating a risk of exposure to contaminants.
Traditional Medicinals is recalling specific lots of Throat Coat Lemon Echinacea tea because raw materials tested positive for Salmonella.
Zimmer Biomet is recalling Humeral Guide Wire Ball Tips because the sterile packaging seal may fail, potentially compromising the device's sterility.
Becton Dickinson is recalling BD Vacutainer Ultra Touch Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.
Ivolution Sports Inc. is recalling IV2 HY-811 motorcycle helmets because they may block peripheral vision, increasing crash risk.
Maharaja Food Importers, Inc. is recalling Whole Wheat Parotta because the label lists ghee but fails to declare milk as an ingredient.
Terumo Cardiovascular Systems Corporation is recalling seven Flowmeter Modules for the Advanced Perfusion System 1 due to inaccurate flow readings that may be difficult to detect.
Premier Kitchen Products is recalling Sharper Image and Frigidaire mandoline slicers because small blades can separate, posing a laceration hazard. No injuries have been reported.
Altec is recalling 2017-2018 EC175, EC225, and EC655 Boom-Mounted Saw vehicles because a valve may allow tree trunks to slip or fall, increasing injury risk.
Mercedes-Benz is recalling 2017 E300, E400, and AMG E43 vehicles because headlight adjustment screws may not be properly sealed, potentially allowing misalignment.
MORryde is recalling 822 Rotational Rubber Pin Boxes because incorrect spindle placement may cause loose bearings, increasing the risk of a crash.
Forest River is recalling 2018 Prime Time WCF35MB trailers because the Federal Placard lists an incorrect Gross Vehicle Weight Rating, which could lead to overloading and increased crash risk.
General Motors is recalling certain 2009-2018 Chevrolet, GMC, and Isuzu vehicles because the installed fire extinguishers may clog or detach, potentially failing to function during a fire.