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.
About 15,616 plastic tip restraint kits supplied with Childcraft furniture sold by School Specialty are being recalled because the straps can break or degrade.
Albertsons store-made Mexican Wedding Cookies, 8 count, are being recalled because the contains statement does not declare pecan. 445 units are affected.
The BD Pyxis MedBank Mini medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Albertsons store-made Cake Pav Chocolate Lady Madeleines Strawberry is being recalled because the contains statement does not declare almond. Six units are affected.
Albertsons store-made Wok Pad Thai Chicken ready meals are being recalled because the contains statement does not declare anchovy.
Exacta Mix Vented Micro-Volume Inlet tubing sets are being recalled because affected lots may contain 0.8-micron filters in place of the validated 3-micron filters.
Albertsons store-made Cookies Cowboy 18 count is being recalled because the contains statement does not declare pecan. 982 units are affected.
CASE v7.0 Cardiac Testing Systems are being recalled because electrical sparking may occur at the printer head, and ignition of thermal paper could cause serious thermal injury.
Straus Family Creamery Mint Chip Organic Super Premium Ice Cream in pints is being recalled over potential contamination with foreign objects, specifically metal pieces.
The BD Pyxis Anesthesia Station ES is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 4,579 units affected.
Betaine Anhydrous 98% distributed by Creative Compounds is being recalled because of possible carbon steel foreign material of 1 to 2 mm. 2,055 kg are affected.
Albertsons store-made Kitchen Salad Grilled Chicken is being recalled because the contains statement does not declare almond. 27 units are affected.
Straus Family Creamery Dutch Chocolate Organic Super Premium Ice Cream in quarts is being recalled over potential contamination with foreign objects, specifically metal pieces.
Albertsons store-made Kitchen Caesar Salads in large and small sizes are being recalled because the contains statement does not declare anchovy. 39 units are affected.
Philips Azurion 3M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
The Da Vinci 5 system tower is being corrected because the near infrared handheld camera can be unintentionally activated when a user tries to turn off illumination.
Kirkland Signature Ultra Strength Antacid, calcium carbonate 1000 mg, made by Guardian Drug Company for Costco, is being recalled over small metallic particles in the tablets.
Lidocaine HCl Injection USP in 5 mL single-dose ampules distributed by Spectra Medical Devices is being recalled for lack of assurance of sterility. 210,625 ampules affected.
Avanta Multi-Patient Administration Tube Sets are being recalled because supplier changes created a fit issue, so the stopcock cannot be reliably engaged with the Contrast Flow Control Valve.
Straus Family Creamery Cookie Dough Organic Super Premium Ice Cream in pints is being recalled over potential contamination with foreign objects, specifically metal pieces.
Aligned Medical AMS16835 Fluids Kits are being recalled because they include Lidocaine Hydrochloride Injection, USP that was recalled by a supplier for quality issues.
Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, are being recalled after failing dissolution specifications, with olmesartan medoxomil content below specification.
Albertsons store-made Platter Cheeses of France is being recalled because the contains statement does not declare almond. 31 units are affected.
Albertsons store-made Gourmet Dubai Cookie is being recalled because the contains statement does not declare pistachio.
Albertsons store-made Muffins Banana Nut Cream Cheese Filled 2 count are being recalled because the contains statement does not declare walnut. Nine units are affected.