Severity 4 of 5
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
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.
Solina U.S. Holding is recalling 459 bags of Ranch Seasoning (Solina 6036195) due to potential Salmonella contamination. The affected bags were distributed in Michigan, Wisconsin, Pennsylvania, Illinois, Georgia, California, and Kansas.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94215T) due to a potential sterile barrier breach. The affected product is a cardiopulmonary bypass vascular catheter distributed worldwide.
Ghirardelli Chocolate Company is recalling its Perfectly Premium Frappe Mix Mocha due to potential Salmonella contamination. Consumers should not consume the product and may return it for a refund.
Shining Sea Fish Co. is recalling MA Cohen's Kippered Herring due to potential Clostridium botulinum contamination. The recall affects vacuum-packed products distributed in Michigan.
Solina U.S. Holding is recalling 161 bags of Solina Crème Fraiche Spice Seasoning due to potential Salmonella contamination. The product was distributed across multiple states.
Ghirardelli Chocolate Company is recalling 50-ounce units of Ghirardelli Sweet Ground Powder White Chocolate Flavored due to potential Salmonella contamination. The product was distributed across the U.S. and internationally.
Ghirardelli Chocolate Company is recalling Perfectly Premium Frappe Mix White Mocha due to potential Salmonella contamination. The affected product was distributed across the U.S., Canada, and select international markets.
Safecor Health, LLC is recalling Atomoxetine HCl 10 mg capsules because some units are incorrectly labeled as 10 mg when they actually contain 25 mg. Patients taking the mislabeled product may receive an incorrect dose.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94725), a cardiopulmonary bypass catheter, because the sterile barrier may be breached, potentially allowing contamination. The cannulas were distributed worldwide.
Good & Gather Mexican Street Corn Trail Mix is being recalled nationwide due to potential Salmonella contamination. Consumers should not eat the product and should return it to the store.
Solina U.S. Holding is recalling 40-pound bags of Garlic Cream Sauce Seasoning due to potential Salmonella contamination. The product was distributed to seven states.
John B Sanfilippo & Sons Inc is recalling Southern Style Nuts Hunter Mix (30 oz jars) distributed nationwide due to potential presence of Salmonella. Consumers should not consume the product.
Solina U.S. Holding is recalling Solina Parmesan Breadstick Sauce Seasoning in 40-pound bags due to potential Salmonella contamination. The product was distributed across seven U.S. states.
Ghirardelli Chocolate Company is recalling its Perfectly Premium Frappe Mix in chocolate flavor due to potential Salmonella contamination. The recall affects 10-lb and 30-lb packages distributed across the United States and internationally.
UCB Biosciences is recalling CIMZIA (certolizumab pegol) prefilled syringes nationwide because of a lack of assurance of sterility. Affected lots are distributed across the US.
Solina U.S. Holding is recalling Solina 6036443 Cheddar Cheese Powder Seasoning (50lb bags) due to potential Salmonella contamination. The product was distributed in Michigan, Wisconsin, Pennsylvania, Illinois, Georgia, California, and Kansas.
Zydus Pharmaceuticals is recalling erythromycin 500 mg tablets nationwide due to the presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit, resulting from manufacturing deviations.
Lil Pick Up Inc. has recalled about 700 Sierra 125U Youth ATVs sold from October 2025 through April 2026 due to defects that violate federal safety standards and pose risks of serious injury or death, including suspension failures, faulty reverse lights, failing brakes, and hot surfaces.
PandaEar is recalling about 9,700 portable hook-on chairs sold online because the crotch restraints can be removed without tools, allowing infants to fall through openings. No injuries have been reported.
Bethlehem Lights 10-inch Illuminated Ribbon Spheres are recalled because the LED lights can overheat and spark, posing a risk of serious injury or death from fire. About 2,000 units sold online through QVC from July 2024 to April 2026 are affected.
ABC Trading is recalling WSDZ Light-up Shot Glasses because the button cell batteries can be easily accessed by children, creating an ingestion hazard that can cause serious internal injuries or death. No injuries have been reported.
Stryker Sustainability Solutions is recalling Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on sterile product packaging, which could compromise sterility and patient safety.
Medline is recalling the Namic Preceptor Manifold due to particulate matter found in the fluid path. The recall affects 760 units distributed in the US and eight other countries.
Medline Industries is recalling multiple cardiac catheterization kits because particulate contamination has been found within the fluid path of the manifolds used in these kits.
Stryker Sustainability Solutions is recalling 90 units of the BARD Dynamic XT Deca Steerable electrophysiology catheter due to incomplete seals on the sterile product.