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.
Boston Scientific is recalling VISIONIST X4 CRT-P Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
New Punjab Sweets Inc. is voluntarily recalling Besan Burfi due to undeclared wheat and milk allergens.
New Punjab Sweets Inc. is voluntarily recalling Laddu in 1 lb. clamshell containers due to undeclared wheat and milk allergens.
Unichem Pharmaceuticals is recalling Divalproex Sodium tablets because metronidazole powder was found in one bottle. The product was distributed nationwide.
Boston Scientific is recalling ALTRUA 2 EL DR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
New Punjab Sweets Inc. is voluntarily recalling 10 lbs of Badusha due to undeclared wheat and milk allergens. The product was distributed in Illinois and Wisconsin.
Philips is recalling specific ECG out and sync cables because electrical interference may cause monitors to misinterpret signals or disable monitoring.
Wayfarer is recalling 2017 24 QW recreational vehicles because the installed Kidde fire extinguishers may clog or detach, potentially failing to function during a fire.
Forest River is recalling 2018 Cherokee recreational trailers because side marker lights are improperly positioned and reflectors may be missing, reducing visibility.
Newmar is recalling 2018 Essex motorhomes because low beam headlights do not illuminate when high beams are activated, reducing driver visibility.
Aston Martin is recalling 2017-2018 DB11 V12 and V8 Coupe vehicles because the driver's frontal air bag may deploy unexpectedly due to insufficient grounding.
Newmar is recalling 2017-2018 Ventana and Dutch Star motorhomes because low beam headlights do not illuminate with high beams, reducing visibility.
KZRV is recalling 2017-2018 Durango Gold recreational trailers because the rear sofa may block the exit window handle, increasing injury risk in emergencies.
Panasonic is recalling 55-inch flat screen televisions with tabletop swivel stands because the mounting screws can loosen, causing the TV to tip over and potentially injure or kill children.
Multipro Baby Cradle N Swings are being recalled because they fail to meet federal safety standards, posing fall and entrapment hazards to babies.
Bed Bath & Beyond is recalling UGG Hudson comforters due to a risk of mold exposure. Consumers should stop using the products and return them for a full refund.
Hillsdale Furniture is recalling Polston and Collin bar stools because the seat can loosen or break off, posing a fall hazard. No injuries have been reported.
Encore Medical is recalling two units of the EMPOWR Tibial Punch because the guide did not sufficiently direct the punch, causing implants to be placed further back than intended.
CareFusion is recalling Alaris Syringe Pump Model 8110 units because the syringe plunger grippers may fail to close automatically, potentially affecting medication delivery.
Cordis Corporation is recalling 511 units of the S.M.A.R.T. Flex Biliary Stent System due to a potential for cracked luer hubs.
Harrisburg Dairies is recalling 365 brand and Harrisburg Dairies brand Egg Nog because dried egg yolks were not listed in the ingredient statement.
Lovebiotics, LLC is recalling The Coconut Cult Mango Cream Probiotic Coconut Yogurt because the allergen statement lists sodium caseinate but fails to identify milk as the source.
Philips is recalling 134 Brilliance iCT SP CT scanners because screws holding the internal gantry may come loose, potentially causing noise.
Encore Medical is recalling two units of the EMPOWR Porous Knee System Tibial Punch because the locking guide failed to properly guide the punch, causing implants to be placed 2-3mm more posterior than intended.
Orthoscan is recalling Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than is visible to the user.