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

✓ Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP). Material Number: 11097543.
Siemens Healthcare recalls Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) tests with material number 11097543 due to potential false low results in patient testing.
Siemens HealthcareAug 11, 2025
✓ Lower riskMedical device
Merge Healthcare, Inc. recalls Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The
Merge Healthcare recalls specific RCSV2 models with software versions 11.1 and 11.1.1 due to pressure sensor errors during high inflation blood pressure tests. Affected units may display 'Pressure Sensor Defective' when initial inflation exceeds 240 mmHg.
Merge HealthcareAug 11, 2025
✓ Lower riskMedical device
Agilent Technologies Denmark ApS recalls Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number:
Dako recalls FLEX Monoclonal Mouse Anti-Human CD20cy (GA60461-2CN) due to potential weak staining causing false negatives in CD20 identification. Affected lots: 41781549, 41762487, 41651581.
DakoAug 11, 2025
✓ Lower riskMedical device
Agilent Technologies Denmark ApS recalls Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number:
Dako recalls FLEX Monoclonal Mouse Anti-Human CD20cy (GA60461-2J) due to potential false negative CD20 staining in immunohistochemistry. Affected lots may lead to incorrect cancer cell classification.
DakoAug 11, 2025

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

Latest recalls

Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP). Material Number: 11097543.

Merge Healthcare, Inc. recalls Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The

Agilent Technologies Denmark ApS recalls Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number:

Agilent Technologies Denmark ApS recalls Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number:

Agilent Technologies Denmark ApS recalls Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number:

Lannett Company Inc. recalls Lisdexamfetamine Dimesylate Capsules, 40 mg, 100-count bottles, Rx Only, Distributed by: Lannett Company, Inc.,

Fromi Usa recalls Brie Royal Faucon; Net Weight about: 2.2lb/ 1kg LOT AUS/US

BMW X6 (2026) recall — Visibility

BMW R 1300 RT (2026) recall — Power Train

Griffith Foods Inc. recalls BISCUIT MIX, SNG 1000042143 NET WEIGHT 2.625 LBS Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road

RIVIAN R1T (2025) recall — Electrical System

FORD MUSTANG (2025) recall — Exterior Lighting

LINCOLN NAUTILUS (2025) recall — Visibility

FORD MUSTANG (2024) recall — Electrical System

LINCOLN CORSAIR (2020) recall — Back Over Prevention

RAYSEARCH LABORATORIES AB recalls RayStation with the following product descriptions: 1. RayStation 2023B, Software Version: 14.0.0.3338. 2. RayStation

RAYSEARCH LABORATORIES AB recalls RayStation with the following product descriptions: 1. RayStation 7, Software Version: 7.0.0.19. 2. RayStation 8A,

Greiner Bio-One North America, Inc. recalls Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2%, REF: 454322

RAYSEARCH LABORATORIES AB recalls RayStation with the following product descriptions: 1. RayStation 12A, Software Version: 13.0.0.1547. 2. RayStation 12A

RAYSEARCH LABORATORIES AB recalls RayStation with the following product descriptions: 1. RayStation 10B, Software Version: 10.1.0.613. 2. RayStation 10B

Medline Industries, LP recalls Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ0382730O; 2) LB BASIC CUSTOM PACK, Model Number:

RAYSEARCH LABORATORIES AB recalls RayStation with the following product descriptions: 1. RayStation 6 Service Pack 1, Software Version: 6.1.1.2. 2.

RAYSEARCH LABORATORIES AB recalls RayStation with the following product descriptions: 1. RayStation 9B, Software Version: 9.1.0.933. 2. RayStation 9B

RAYSEARCH LABORATORIES AB recalls RayStation with the following product descriptions: 1. RayStation 11A, Software Version: 11.0.0.951. 2. RayStation 11A

Medline Industries, LP recalls Sterile Medline Convenience Kits: 1) EXTREMITY PACK, Model Number: DYNJ45701B

Schiller, Ag recalls Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006

Philips Medical Systems Nederland B.V. recalls IntelliSpace Cardiovascular, Software 8.0.0.4.

RAYSEARCH LABORATORIES AB recalls RayStation with the following product descriptions: 1. RayStation 8B, Software Version: 8.1.0.47. 2. RayStation 8B

RAYSEARCH LABORATORIES AB recalls RayStation with the following product descriptions: 1. RayStation 11B, Software Version: 12.0.0.932. 2. RayStation 11B

Baxter Healthcare Corporation recalls Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8