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.
Paleteria La Jalpita is recalling Gelleta (Cookies) popsicles due to undeclared soy lecithin and wheat. The product was distributed in Oregon and Washington.
Inn Foods Inc. is recalling IQF Italian Cut Green Beans after a sample tested positive for Listeria monocytogenes.
Cowden's Lycoming Bakery is recalling 123 units of 2-pack pizza shells because they contain whey, a milk allergen, that was not listed on the label.
Mondelez International is recalling Nabisco Fig Newtons because the outer carton fails to declare milk, a major allergen, while the inner packaging does.
The Apothecary Shoppe is recalling S-Methylcobalamin 1000 mcg/mL Injection because documentation for environmental monitoring during production was missing.
Siemens Medical Solutions is recalling Biograph 64-3R TruePoint systems because they may be missing a locking ring on optional ceiling mounts.
Winnebago is recalling 2014-2015 Itasca and Winnebago motorhomes because deadbolt locks may become stuck, potentially trapping occupants inside the vehicle.
Siemens Medical Solutions USA Inc. is recalling one Biograph mCT S(64)-4R unit because it may be missing a locking ring on the optional ceiling mount.
The Apothecary Shoppe LLC is recalling SO-Acetylcysteine 10% Sterile Ophthalmic Solution due to lack of documentation for environmental monitoring during production.
Philips is recalling 13,168 HeartStart XL+ defibrillators worldwide due to software and hardware issues that can affect device function.
Strick Trailers is recalling 2013 Dry Freight Van Trailers because the tires are positioned too far forward, failing to meet federal rear impact protection standards.
Breezer is recalling about 1,700 Downtown bicycles because pedals can separate from the spindle, posing a crash hazard. No injuries have been reported.
Britax is recalling specific ClickTight child seats because a red harness adjuster button may stick, allowing the shoulder harness to loosen and increasing injury risk in a crash.
Nissan is recalling 2015 Armada vehicles because front seat belt buckles may not latch or unlatch properly, increasing crash injury risk.
Subaru is recalling 2015-2016 Legacy and Outback vehicles because a deformed seal cap may allow transmission oil to leak onto the exhaust pipe, creating a fire risk.
Keystone RV Company is recalling certain 2014-2016 Avalanche, Alpine, and Laredo models because a rear window labeled as an emergency exit may be blocked by a ladder.
Forest River is recalling 2014-2015 Vengeance vehicles because the gross vehicle weight rating on the certification label is incorrect, which could lead to vehicle overloading.
Precious Cargo is recalling infant one-piece garments because the snaps can detach, posing a choking hazard to young children. No injuries have been reported.
Volvo is recalling 2016 XC90 vehicles because third-row side curtain air bags may not fully inflate, increasing injury risk in a crash.
The Children's Place is recalling boys' varsity jackets because metal snaps could detach and pose a choking hazard to young children.
Turtle Top is recalling certain 2012 Van Terra XL and Odyssey XL transit buses because their windows may not meet federal safety loading requirements.
Philips is recalling 159 Ingenuity CT scanners due to software errors affecting dose control, image artifacts, and heart rate measurement.
The Anspach Effort, Inc. is recalling 70 G1 dissection tools because the shaft exposure may be greater than labeled when used with certain attachments.
Atkins Nutritionals is voluntarily recalling specific cartons of Atkins Chocolate Candies because they may contain sachets of Atkins Peanut Candies.
EXP Pharmaceutical Services Corp is recalling TAUT Intraducer Peritoneal Catheters because the company failed to register as a medical device establishment or maintain its own quality system.