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.
Benlan, Inc. is recalling specific lots of 8 FR pediatric feeding tubes that may be packaged with 5 or 6.5 FR tubes instead.
Corflex is recalling specific Post-Operative Knee Braces because they may fail to maintain a locked position, potentially causing loss of balance or unwanted knee movement.
Corflex is recalling specific models of the Hailey Ortho Contender Post-Op Knee Brace because they may fail to maintain a locked position, risking loss of balance or unwanted joint movement.
Cost Plus World Market is recalling Tovin chairs because the legs can bend or break, posing a fall hazard. No injuries have been reported.
Walmart is recalling Rival brand electric griddles because the heating element can crack, allowing water to enter and posing a shock hazard.
Pier 1 Imports is recalling Swingasan chairs and stands because the suspension hardware can break or the stand can tip over, posing a fall hazard.
Gulf Stream is recalling 662 motor homes because a bolt on the electric steps may fracture, causing the steps to become unstable and increasing the risk of injury.
Transportation Collaborative is recalling 257 model year 2015 Trans Tech school buses because a reflective decal on the stop arm may peel loose, reducing visibility.
New York Style Sausage Co. is recalling approximately 4,040 pounds of pork sausage because the products use sheep casings that are not declared on the label, posing an allergy risk.
Britax is recalling specific B-Safe 35 infant car seats because the carry handles may crack and fracture, posing a risk of injury if the seat falls.
Blue Bird is recalling 2016-2017 Vision and All American school buses because stop arm reflective decals may peel off, reducing visibility to other drivers.
Office Depot is recalling Crawley II executive chairs because the seat plate weld can break, posing a fall hazard. No injuries have been reported.
Zulily is recalling about 450 children's pajamas that do not meet federal flammability standards, posing a risk of burn injuries.
Walgreens Infusion Services is recalling Tobramycin 620 mg/NS 100 mL Accuflo bags in Texas due to a lack of assurance of sterility.
Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA tubes because some were manufactured with insufficient EDTA additive, which may lead to erroneous platelet results.
Walgreens Infusion Services is recalling 14 L-Cysteine 800 mg syringes in Texas because the agency could not ensure the product was sterile.
Aesculap is recalling 41 Valve XS Atrium Retractor blades distributed in New York because corrosion was found on a ball joint caused by incorrect manufacturing materials.
Barilla America NY, Inc. is recalling specific lots of Barilla Medium Shells pasta due to the presence of aluminum fragments.
Barilla America NY, Inc. is recalling specific lots of foodservice Penne Rigate pasta due to the presence of aluminum fragments.
Walgreens Infusion Services is recalling 23 insulin syringes in Texas due to a lack of assurance of sterility.
Walgreens Infusion Services is recalling 19 bags of Milrinone 0.375 mcg/kg/min D5W in Texas due to a lack of assurance of sterility.
Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA tubes because some were manufactured with insufficient EDTA additive, which may lead to erroneous platelet results.
Beckman Coulter is recalling MicroScan Pos Combo panels that may produce falsely negative Voges-Proskauer results for Staphylococcus aureus.
Trumpf Medical Systems is recalling 20,713 ceiling-mounted surgical light systems because the spring arm can detach, causing the light head to fall.
Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA blood collection tubes because some were manufactured with insufficient EDTA additive, which may lead to erroneous platelet results.