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.
Northern Tier Bakery, LLC is recalling approximately 905 pounds of ready-to-eat salad products sold in Minnesota and Wisconsin due to possible Listeria monocytogenes contamination.
Forest River is recalling 2022 Prime Time Crusader and Sanibel fifth wheel travel trailers because step treads may detach, increasing injury risk.
About 16,000 Intimidator and Mahindra utility vehicles (UTVs) are being recalled because the throttle cable can freeze in cold temperatures, causing a stuck throttle and brake failure. Additionally, certain Model Year 2022 Intimidator GC1K vehicles lack speed-limiting software when the seatbelt is disengaged.
Hisense USA is recalling about 55,200 French door refrigerators because the door hinge can break and cause the door to detach, posing an impact injury hazard. The firm has received reports of five injuries including foot bruises and lacerations.
Roush CleanTech is recalling specific LPG fuel return lines installed on vehicles in 24 states and D.C. due to a corrosion risk that could cause fuel leaks and fire.
Ferrara is recalling 2021-2023 Inferno and Igniter vehicles because a defective circuit board can cause lighting to fail, increasing crash risk.
Certain 2022 RAM 1500, 2500, and 3500 pickup trucks may have defective radio software that prevents the rearview camera image from displaying, reducing rear visibility and increasing crash risk.
Spirit Halloween is recalling about 12,400 units of 48-inch black light fixtures sold from August to November 2021. The bulb can pop, flash, overheat, and catch fire, posing fire and burn hazards.
Jungle Jumparoo children's toys sold online from November 2018 through March 2019 contain yellow poles with lead levels exceeding the federal ban. Lead is toxic if ingested and can cause adverse health effects in young children.
Chrysler is recalling specific Mopar high-pressure fuel pumps and 3.0L diesel engines because pump failure may cause fuel starvation and loss of drive power.
Tornier's Ratcheting Screwdriver Handle in the Aequalis Perform Reversed kit cannot meet sterilization requirements when sterilized per instructions in an Aesculap container. The company is recalling 1066 units distributed nationwide.
Becton Dickinson is recalling 199 units of BD Anti-Kappa PE flow cytometry reagent because samples may exhibit uncharacteristic flow profiles that could affect test accuracy.
Busse Hospital Disposables is recalling CVC Dressing Change Kits nationwide due to uncertainty about test method validation during manufacturing. Affected swab products may not have been adequately validated for sterility and efficacy.
Direct Rx is recalling 81 bottles of Losartan Potassium and Hydrochlorothiazide 100/12.5 mg due to AZIDO impurity exceeding acceptable manufacturing standards. Affected bottles were distributed in Alabama, Georgia, Florida, and Louisiana.
Nephron Sterile Compounding Center is recalling Phenylephrine HCl Injection syringes nationwide due to lack of assurance of sterility affecting 76,860 units.
Busse Hospital Disposables recalls approximately 425 units of its Single Shot Epidural Tray nationwide due to inadequate validation of manufacturing test methods for swab components.
Intuitive Surgical recalls da Vinci Energy SynchroSeal surgical instruments due to potential seal failure. Excessive tissue in the instrument jaws can result in insufficient sealing.
Nephron Sterile Compounding Center is recalling 134,415 pre-filled syringes of Epinephrine Injection due to lack of assurance of sterility. Affected lots were distributed nationwide; patients and providers should contact their healthcare provider.
Busse Convenience kits containing swab/swabstick drug products manufactured by Professional Disposables International are being recalled due to uncertainty about manufacturing test method validation.
Busse Convenience kits containing swab/swabstick drug products manufactured by Professional Disposables International (PDI) have been recalled due to uncertainty regarding the adequacy of manufacturing test method validation.
Nephron Sterile Compounding Center has recalled 115,640 units of Labetalol HCl Injection due to lack of assurance of sterility. The affected product was distributed nationwide.
Walnut Creek Chocolate Co Inc is recalling Jason & Mary Large Dark Peanut Butter Cups due to potential Salmonella contamination affecting 4740 units across 30 states.
The Proteus235 Proton Therapy System may deliver radiation to initial treatment fields with incorrect scanning magnet settings. The radiation field may be smaller than expected and may deliver higher dose than prescribed.
Nephron Sterile Compounding Center recalled Lidocaine HCl Injection due to lack of sterility assurance. The recalled lot affects 65,590 pre-filled syringes distributed nationwide.
Nephron Sterile Compounding Center is recalling 35,850 pre-filled syringes of EPINEPHrine Injection due to lack of sterility assurance. The affected syringes were distributed nationwide.