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

76,847 found

⚠️ Use cautionVehicle
FORD ESCAPE (2020) recall — Visibility
Ford recalls 2020 Escape vehicles with faulty wiper motors that may stop working, increasing crash risk. Owners must have wiper motors inspected and replaced by dealers.
FordMar 3, 2026
⚠️ Use cautionMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
PHILIPS recalls ALLURA Xper FD10 X-ray systems with specific system codes (722003, 722010, 722026) due to potential failure to initiate X-ray imaging when using the wired foot switch.
PHILIPSMar 3, 2026
✓ Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
Philips recalls Azurion 7 B12 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch.
PhilipsMar 3, 2026
✓ Lower riskMedical device
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C; System Code: 722001;
Philips recalls Allura Xper FD10C X-ray systems with system code 722001 due to potential failure to initiate X-ray imaging when using the wired foot switch. Affected units may require repair to ensure safe operation.
PhilipsMar 3, 2026
✓ Lower riskMedical device
Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided; SOFT-VU HH1 4F X 100CM 038 NB 0SH; Catalog No.: 10714040;

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

Latest recalls

FORD ESCAPE (2020) recall — Visibility

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD10C; System Code: 722001;

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided; SOFT-VU HH1 4F X 100CM 038 NB 0SH; Catalog No.: 10714040;

Angiodynamics, Inc. recalls Soft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 NB 0SH; Catalog No.: 10710013;

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 65CM 038 NB 0SH; Catalog No.: 10714011;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20; System Code: 722038;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/15; System Code: 722058;

Angiodynamics, Inc. recalls AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 100CM 038 NB 0SH; Catalog No.: 10714018;

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Sos Omni Selective (1), Non-Braided; SOFT-VU SO1 4F X 80CM 038 NB 0SH; Catalog No.:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Straight Art, Non-Braided; SOFT-VU STR ART 4F X 65CM 035 NB 0SH; Catalog No.: 10731401;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/20 OR Table; System Code: 722039;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 100CM 035 NB 10SH; Catalog No.: 10707103;

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 035 NB 6SH; Catalog No.: 10732301;

Angiodynamics, Inc. recalls AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers; ACCU-VU PT 4F X 70CM 035 NB 10SH 21 R/O 1CM;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 038 NB 0SH; Catalog No.: 10714017;

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 65CM 038 NB 0SH; Catalog No.: 10714009;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20/10; System Code: 722029;

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 038 NB 6SH; Catalog No.: 10714001;

Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB 0SH; Catalog No.: 10734301; Product/UPN