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.
Centurion Medical Products is recalling 80 units of Universal Line Full Body Drape Kits due to incomplete sterile packaging seals that may compromise product sterility.
Baxter Healthcare is recalling 336 Prismaflex Control Units with software versions below 7.21 due to communication error alarms that may interrupt therapy or cause blood loss.
Western / Scott Fetzer Company is recalling 25,840 Grab n Go Opti VIPR systems because the control knob may rotate beyond its functional range, limiting access to flow settings.
Becton Dickinson is voluntarily recalling MaxZero Extension Sets with Needle-less Connectors because fluid droplets may separate from the sealed surface after disconnection.
Zimmer Biomet is recalling 5,459,583 periarticular shoulder plates because non-highly polished implants may adhere to the LDPE bag packaging.
Argon Medical Devices is recalling Septishield II products because an incomplete seal may cause a loss of sterility.
Argon Medical Devices is recalling Hemostasis Valves because incomplete pouch seals may cause a loss of sterility.
Argon Medical Devices is recalling Vascuclamp radiopaque vascular clamps because an incomplete pouch seal may cause a loss of sterility.
Pride of Iowa Sandwiches is recalling J. BOS Vending Service Monster Cheeseburgers because the beef patties used in them may contain foreign metal material.
Argon Medical Devices is recalling Double Male LL Adapters because an incomplete pouch seal may cause a loss of sterility.
Pride of Iowa Sandwiches, Inc. is recalling Market Choice Monster Cheeseburgers because the beef patty ingredient was potentially contaminated with foreign metal material.
Hitachi Medical Systems America Inc is recalling 39 Scenaria Whole-body X-ray CT Systems because cables to the controller unit may not be affixed properly, creating a risk of detachment during scanning.
Matrix Headgear is recalling Alpha motorcycle helmets because the retention system may fail, allowing the helmet to separate from the head during a crash.
Ford is recalling 2018-2019 F-250, F-350, and F-450 Super Duty trucks because daytime running lights may not dim, increasing crash risk.
Hooey is recalling about 6,600 children's sweatshirts with hood drawstrings due to a strangulation hazard. No injuries have been reported.
USDA FSIS issued a public health alert for specific ready-to-eat entrees containing ingredients recalled by Mann's Packing Co. due to possible Listeria monocytogenes contamination.
Skylight is recalling Series I power adapters sold with digital photo frames because the casing can break, exposing metal prongs and posing an electrical shock hazard.
NHTSA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because a fuel system defect may cause diesel leaks or fuel overflow.
Hyundai is recalling 2020 Palisade vehicles because mounting bolts may damage side curtain air bags, potentially preventing proper inflation in a crash.
General Motors is recalling 2014-2016 Chevrolet SS vehicles because corrosion in the steering connector may cause a loss of electric power steering assist, increasing the risk of a crash.
Thor Motor Coach is recalling specific Tuscany and Venetian motorhomes because rear reflectors may be positioned too high, reducing vehicle visibility and increasing crash risk.
TIDI Products is recalling Posey Connected Twice-As-Tough Cuffs because they do not meet design specifications. The recall affects 7,692 units distributed in the US and internationally.
Valeritas is recalling DEMO No Needle Corrugated Cartons because they may contain a needle. The recall covers 49,074 units distributed nationwide.
Rong Shing Trading Inc. is recalling Ganchi Naiweitangpian Candy because it contains undeclared milk. The product was distributed to retailers in seven states.
Draeger Medical Systems is recalling 5,634 Infinity Acute Care System monitors due to cybersecurity vulnerabilities that may cause device reboots and loss of alarm functionality.