Official U.S. recalls · explained plainly

Know if it’s recalled — and exactly what to do.

We pull official government recall records and translate each one into plain language: what happened, how serious it is, and the steps to take. No legalese.

Search by meaning, not just keywords — describe the product or the hazard and we’ll find matching recalls even when the official notice uses different words. Brand names and model numbers work too.

Latest recalls

76,887 found

⛔ Stop using nowConsumer product
URMYWO Baby Loungers Recalled Due to Risk of Serious Injury or Death from Suffocation and Fall Hazard; Violates Mandatory Standard for Infant Sleep Products; Sold on Amazon by Pomona
URMYWO baby loungers with model UMCZC01AE recalled due to suffocation and fall risks. Remove sleeping pad, cut sides, email photo for refund. Sold on Amazon by Pomona.
URMYWOSep 4, 2025
⛔ Stop using nowConsumer product
StopBox USA Recalls AR-15 Chamber Lock Pros Due to Risk of Serious Injury and Death
StopBox USA recalls certain AR-15 Chamber Lock Pro firearm locks sold between June 2 and July 15, 2025, due to a defect allowing unauthorized access that could cause serious injury or death.
StopBox USASep 4, 2025
⛔ Stop using nowConsumer product
Makita U.S.A., Inc. Recalls Cordless Grease Guns and Grease Gun Hoses Due to Laceration Hazard
Makita recalls cordless grease guns and hoses with model numbers XPG01S1, XPG01SR1, XPG01Z and specific hoses due to a laceration hazard from grease ejection through a potential hole in the hose.
MakitaSep 4, 2025
⚠️ Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; Product Code: 722029; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979,
Philips recalls Allura Xper FD20/10 X-ray systems due to potential motor failure from internal component deterioration. Affected units may lose motorized movements but manual adjustments and imaging remain functional.

Know if it’s recalled — and exactly what to do.

Latest recalls

URMYWO Baby Loungers Recalled Due to Risk of Serious Injury or Death from Suffocation and Fall Hazard; Violates Mandatory Standard for Infant Sleep Products; Sold on Amazon by Pomona

StopBox USA Recalls AR-15 Chamber Lock Pros Due to Risk of Serious Injury and Death

Makita U.S.A., Inc. Recalls Cordless Grease Guns and Grease Gun Hoses Due to Laceration Hazard

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; Product Code: 722029; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; Product Code: 722038; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Product Codes: (1)722012, (2) 722028, (3) 722006; Associated 510(k) numbers: K102005, K130842,

Beckman Coulter Inc. recalls SYNCHRON Systems Phosphorus (PHOSm) Reagent REF: 467868 For In Vitro Diagnostic Use, Rx Only.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10/10; Model Numbers: (1) 722005, (2) 722011, (3) 722027; Associated 510(k)s: K102005, K130638, K130842,

Inpeco S.A. recalls FlexLab (FLX) System. Potassium Test System. in vitro diagnostic

Inpeco S.A. recalls FlexLab X (FXX) System. Potassium Test System. in vitro diagnostic

Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20; Model Numbers: (1) 722006, (2) 722012, (3) 722028; Associated 510(k)s: K102005, K130638, K130842,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane OR Table Product Codes: (1)722020, (2) 722025; Associated 510(k) numbers: K102005, K130842,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 OR Table; Model Numbers: (1) 722015, (2) 722023, (3) 722035; Associated 510(k)s: K102005, K130638,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15 OR Table; Model Numbers: 722059; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Cardio Vascular-Allura Centron; Model Numbers: 722400; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20 OR Table; Product Code: 722039; Associated 510(k) numbers: K102005, K130842, K130638, K133292,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; Model Numbers: 722038; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane; Model Numbers: (1) 722008, (2) 722013; Associated 510(k)s: K102005, K130638, K130842,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 OR Table Product Codes: (1)722023, (2) 722035, (3) 722015; Associated 510(k) numbers: K102005,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper CV20; Model Numbers: 722031; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane OR Table; Model Numbers: (1) 722020, (2) 722025; Associated 510(k)s: K102005, K130638,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbers: K102005, K130842,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura CV20; Product Code: 722031; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10 OR Table; Model Numbers: 722033; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20 OR Table; Model Numbers: 722039; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; Model Numbers: 722029; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15; Model Numbers: 722058; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859,

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10; Model Numbers: (1) 722003, (2) 722010, (3) 722026; Associated 510(k)s: K102005, K130638, K130842,