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.
Resource Optimization & Innovation LLC is recalling 120 sterile custom procedure trays because the included light gloves can split, breaking the sterile field.
Cumberland Valley Creamery is recalling Luqman Cheese, Yellow Colby Buffalo, because laboratory analysis found levels of E. coli exceeding allowed limits.
Resource Optimization & Innovation Llc is recalling 436 Regard custom procedure trays because a light glove component can split, breaking the sterile field.
Resource Optimization & Innovation LLC is recalling 350 Regard custom procedure trays because a light glove component can split, breaking the sterile field.
Mylan Pharmaceuticals is recalling Atorvastatin Calcium Tablets 20 mg due to potential microbial contamination and elevated bioburden.
Resource Optimization & Innovation LLC is recalling 189 custom procedure trays because the included light gloves can split, breaking the sterile field.
Resource Optimization & Innovation LLC is recalling 18 sterile total hip procedure trays because a light glove component can split and break the sterile field.
Resource Optimization & Innovation LLC is recalling 156 Regard custom procedure trays because the included light gloves can split, breaking the sterile field.
Mylan Pharmaceuticals is recalling specific lots of Atorvastatin Calcium 40 mg tablets due to potential microbial contamination and elevated bioburden.
Resource Optimization & Innovation LLC is recalling 92 sterile robotic laparoscopic procedure trays because a light glove component can split, breaking the sterile field.
Resource Optimization & Innovation Llc is recalling 1,056 sterile procedure trays because a light glove component can split and break the sterile field.
Resource Optimization & Innovation LLC is recalling 28 sterile pacemaker procedure kits because the included light gloves can split, breaking the sterile field.
Forest River is recalling 2016-2018 XLR Toyhaulers because weak fasteners may allow the side patio deck to drop unexpectedly, increasing crash risk.
Gulf Stream is recalling 2011-2017 Amerilite trailers because incorrect weight information on the Federal Placard may lead to overloading and increased crash risk.
Fred Meyer is recalling approximately 48,000 children's hooded sweatshirts and girls bomber jackets because the zipper pull can detach, posing choking and laceration hazards.
Safavieh is recalling about 500 Audrey lingerie chests because they can tip over and entrap children if not anchored to the wall.
Newmar is recalling 2017 King Aire motorhomes because improperly seated headlight harness seals may allow water entry, causing the dash display to obscure speedometer and RPM readings.
Rexon is recalling Black+Decker portable table saws sold at Walmart because the stand can collapse, posing laceration and impact injury risks.
BMW is recalling 2016-2017 MINI Cooper Clubman vehicles because the inner brake light may fail to illuminate when turn signals are active, increasing crash risk.
Forest River is recalling 2017 Salem and Wildwood recreational vehicles because the Federal Placard lists an incorrect Gross Axle Weight Rating, which could lead to overloading.
Sock and Accessory Brands is recalling John Deere infant caps because the top button can detach, posing a choking hazard to young children.
humangear is recalling capCAP bottle caps because they may leak or dislodge, posing a burn hazard when used with hot liquids. No injuries have been reported.
BlenderBottle is recalling Whiskware glass dressing shaker bottles because the glass bottom can break when struck by the metal agitator, posing a laceration hazard.
CareFusion is recalling Alaris System PC units because low battery alarms may fail to trigger before the battery discharges, stopping all infusion channels.
Lakeside Foods is voluntarily recalling specific frozen peas and carrots products due to potential Listeria monocytogenes contamination.