Hazard
1,189 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 1,189 foreign object recalls we have scored against our rubric, 24 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 202 (17%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all foreign object recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
Justin's Nut Butter is voluntarily recalling specific lots of Maple Almond Butter and Chocolate Hazelnut Butter due to the presence of foreign metallic fragments.
Genzyme Corporation is recalling LeGoo Endovascular Occlusion Gel 2.5 mL because the product contains particulates (fibers). The recall covers 100 units distributed worldwide.
Justin's Nut Butter is voluntarily recalling specific lots of Maple Almond Butter and Chocolate Hazelnut Butter due to the presence of foreign metallic fragments.
Hospira is recalling 264,432 bags of 0.9% Sodium Chloride Injection because the product may contain fibrous material.
Global Juices & Fruits LLC is recalling Nature's Earthly Choice Organic Quinoa because it may contain sand and grit.
Sorin Group is recalling Edwards Lifesciences Suction Wand Model S099B because plastic particles were found inside the packaging pouch.
Hospira is recalling 94,110 vials of Propofol Injectable Emulsion because a single stainless steel particulate was found during inspection.
Hospira Inc. is recalling 0.9% Sodium Chloride Injection, USP, 1000 mL containers due to the presence of small grey/brown brass particulates.
GlaxoSmithKline is recalling TUMS Ultra Assorted Berries 1000mg chewable tablets because they may contain foreign TUMS 750mg tablets.
American Importing Co. is voluntarily recalling specific packages of 16 oz Vanilla Almond Granola because they may contain pliable metal wire mesh fragments from a defective flour sifter.
American Importing Co. is voluntarily recalling 16 oz Vanilla Almond Granola packages that may contain pliable metal wire mesh fragments from a defective flour sifter.
American Importing Co. is voluntarily recalling 16 oz Vanilla Almond Granola packages that may contain pliable metal wire mesh fragments from a defective flour sifter.
Church & Dwight is recalling specific lots of Sodium Bicarbonate, USP, used in medical devices and drugs due to metal and other contamination.
Staar Surgical is recalling nanoFLEX and Afinity intraocular lenses because glass particles may be present in the storage vials.
Edwards Lifesciences is recalling specific models of rigid suction wands because plastic particulate was found inside the sterile pouch and within the wand.
Staar Surgical is recalling specific Afinity and nanoFLEX intraocular lenses because glass particles may be present in the storage vials.
Church & Dwight is recalling Arm & Hammer Sodium Bicarbonate Powder due to the presence of stainless steel and other foreign substances.
Alymaq Inc is recalling 770 bags of Extra Fine Granulated Sugar AIB in Ohio due to the potential presence of plastic fragments.
The FDA is recalling 23,050 units of Versaport Bladeless Optical Trocars because seals may disengage, potentially causing components to enter the patient's cavity.
HP Hood LLC is recalling 4% cottage cheese under multiple brands due to the possible presence of metal fragments. The product was distributed in 21 states.
Nestle is recalling specific California Pizza Kitchen Crispy Thin Crust White pizzas because they may contain fragments of clear plastic.
Grippo Potato Chip Co. is recalling Bar-B-Q flavored potato chips after an inspection found metal fragments in the salt hopper.
Cardinal Health is recalling 4,571 Presource Shoulder Procedure Kits because plastic packaging remnants may obstruct airflow in the filter.
Cardinal Health is recalling 4,571 Presource Shoulder Arthroscopy Kits because plastic packaging remnants may obstruct airflow in the filter.
Cardinal Health is recalling 4,571 Presource PBDS kits because plastic packaging remnants may lodge in the filter and obstruct airflow.