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.
Nature's Eudos Distributors LLC is recalling Eudos Bronquilan due to undeclared food color additives (FD&C Yellow #5, FD&C Blue #1, and FD&C Red #40). Consumers with allergies or sensitivities to these dyes should not use the product.
South Asian Food Inc. is recalling Bengal King Family Pack Vegetable Singara due to undeclared peanut, a major allergen that poses a serious risk to consumers with peanut allergies.
Mozarc Medical is recalling MAHURKAR Chronic Hemodialysis Catheter Sport Pack units due to a potential breach in sterile barrier packaging that could compromise the product's sterility.
Mozarc Medical US LLC is recalling Palindrome Precision Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. Affected units were distributed worldwide including the US, Canada, and Mexico.
Silex Medical recalls the Signature Laparoscopic Sharp Tooth Grasper due to incomplete insulation on the shaft near the rotator wheel, which creates an electrical hazard during use.
Luminex is recalling VERIGENE Gram Negative Blood Culture test cartridges due to a consumable issue that may produce incorrect results on a small portion of one lot.
Bedner Growers, Inc. is recalling cucumbers shipped from May 3–12, 2025, due to potential Salmonella contamination. Affected products were distributed in Florida in cardboard boxes of 24, 36, or 68 count.
Torrent Pharma Inc. is recalling Fluoxetine Tablets USP 20 mg due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit. The affected lot is distributed nationwide.
Beckman Coulter is recalling the Access Testosterone assay (Catalog Number 33560) due to inadequate maintenance on manufacturing equipment that caused cross-contamination in testosterone reagent packs, which could result in inaccurate patient test results.
New Grains Gluten Free Bakery is recalling Dye-Free Frosted Sugar Cookies due to printing quality issues that failed to clearly declare allergens (egg, milk, soy) on the label. The product was distributed in Utah.
Nova Bus is recalling certain 2022-2023 LFS buses because a digital display firmware error may leave the instrument panel turn signal indicators solidly lit, failing FMVSS 108.
Mozarc Medical is recalling Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. The affected catheter models were distributed nationwide in the US and in Canada and Mexico.
Rivian is recalling certain 2025 R1S and R1T vehicles because one or both front turn signals may fail to illuminate and flash, failing FMVSS 108. 27,882 units affected.
Mexquisite, Inc. is recalling Salsa Cilantro in 8.5lb plastic jugs due to potential foreign object contamination. The product was distributed to Texas and California.
Mozarc Medical US LLC is recalling Palindrome Precision SI Chronic Hemodialysis Catheters (Sport Pack) due to a potential breach of sterile barrier packaging. Approximately 95,938 units distributed nationwide and in Canada and Mexico are affected.
Silex Medical is recalling 8 units of Signature Laparoscopic Debakey Grasper instruments (Model 5862100) due to incomplete insulation on the shaft near the rotator wheel, which could expose the user or patient to electrical contact.
NEW GRAINS GLUTEN FREE BAKERY is recalling Cinnamon Raisin Bagels (16 oz, 4-count packages) due to poor label printing that fails to clearly declare the presence of egg allergen.
Hyundai Translead is recalling 2026 Dry Van Trailers because insufficient lubrication on the liftgate cylinder pin may cause it to seize, leading to liftgate failure and injury risk.
Forest River is recalling certain 2025 Salem and Wildwood travel trailers because the side entry gate latch may unlock, allowing the strut to open the gate during transit.
Mack Trucks is recalling 2025 Anthem and Granite vehicles because improperly routed power cables may cause electrical shorts, leading to engine stalls or fires.
Braun is recalling 1,533 Chrysler Pacifica, Voyager, and Toyota Sienna vehicles because seat belt tie-down fasteners may be loose, increasing injury risk in crashes.
Ford is recalling 2025 Maverick vehicles because the air bag indicator light may be loose or dislodged, potentially failing to warn occupants of a deactivated air bag.
Mercedes-Benz is recalling certain 2023–2025 GLC 300 and GLC 300 4MATIC, 2024–2025 AMG GLC 43 4MATIC, 2025 GLC 350E 4MATIC, and 2025 AMG GLC 63 S E vehicles with panoramic sunroofs. The C-pillar may not absorb adequate impact in a crash, increasing injury risk.
Harley-Davidson is recalling certain 2018–2024 Softail motorcycles because the rear shock pre-load adjuster mounting tab may break and damage the tire, causing sudden loss of pressure and increasing crash risk.
Midea is recalling about 1.7 million U and U+ Window Air Conditioners because pooled water can fail to drain quickly, allowing mold to grow. At least 152 mold reports exist, including 17 reports of consumers experiencing respiratory infections, allergic reactions, coughing, sneezing, and sore throats.