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

76,900 found

✓ Lower riskMedical device
SEDECAL SA recalls Model Number 40KWFXPLUS-710CW.007, Mobile X-ray system
SEDECAL recalls mobile X-ray system model 40KWFXPLUS-710CW.007 due to non-water resistance requiring strict cleaning per manual to prevent damage.
SEDECALJun 10, 2025
✓ Lower riskMedical device
SEDECAL SA recalls Model Number 40KW-FX.899, Mobile X-ray system
SEDEC: Mobile X-ray system model 40KW-FX.899 not water-resistant; improper cleaning risks damage. Affected units have specific serial numbers and UDI/DI codes.
SEDECALJun 10, 2025
ℹ️ UnratedMedical device
Boston Scientific Corporation recalls VersaCross RF Wire (VXW). Indicated for creation of an atrial septal defect in the heart. Product ID VXW0002 Device
Boston Scientific recalls VersaCross RF Wire (VXW0002) due to potential hole in sterile pouch risking infection. Affected units sold only in Japan. No remedy stated in recall notice.
Boston ScientificJun 10, 2025
✓ Lower riskMedical device
Boston Scientific Corporation recalls VersaCross Access Solution (VXSK), Product Description and ID: VXSK (180J RF WIRE 63CM/45DEG/D0) VXSK0101 VXSK (180J RF
Boston Scientific recalls VersaCross Access Solution (VXSK) products due to potential hole in sterile barrier pouch, risking infection. Affected units include specific model IDs and batch numbers listed in the recall notice.
Boston ScientificJun 10, 2025
✓ Lower riskMedical device
SEDECAL SA recalls Model Number SM-40HF-B-D-C; 40KW.002, Mobile X-ray system

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

Latest recalls

SEDECAL SA recalls Model Number 40KWFXPLUS-710CW.007, Mobile X-ray system

SEDECAL SA recalls Model Number 40KW-FX.899, Mobile X-ray system

Boston Scientific Corporation recalls VersaCross RF Wire (VXW). Indicated for creation of an atrial septal defect in the heart. Product ID VXW0002 Device

Boston Scientific Corporation recalls VersaCross Access Solution (VXSK), Product Description and ID: VXSK (180J RF WIRE 63CM/45DEG/D0) VXSK0101 VXSK (180J RF

SEDECAL SA recalls Model Number SM-40HF-B-D-C; 40KW.002, Mobile X-ray system

SEDECAL SA recalls SHIMADZU RF.004, Mobile X-ray system

SEDECAL SA recalls Model Number SM-20HF-Batt; 20KW ANALOG, Mobile X-ray system

SEDECAL SA recalls SM_40HF_BDC3, Mobile X-ray system

SEDECAL SA recalls SM_40HF_B_D_VIR3, Mobile X-ray system

SEDECAL SA recalls Model Number SM-40HF-B-D-C; 40KW 70C, Mobile X-ray system

SEDECAL SA recalls Model Number SM-40HF-B-D-C; 40KW, Mobile X-ray system

Boston Scientific Corporation recalls Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F 63CM 45DEG TF85-32-63-55 TORFLEX 8.5F 63CM

SEDECAL SA recalls Model Number SM-40HF-B-D-C; 40KW 55C/60C, Mobile X-ray system

SEDECAL SA recalls Model Number 40KWFXPLUS.004, Mobile X-ray system

SEDECAL SA recalls Model Number SM-32HF-B-D-C; 32KW 50G, Mobile X-ray system

Boston Foundation For Sight recalls BostonSight PROSE Lens.

Boston Foundation For Sight recalls BostonSight SCLERAL Lens

SEDECAL SA recalls MobileDiagnost wDR 2.2; Model Number REF 9890-010-89522, Mobile X-ray system

IMMUNOCORE, LLC recalls KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion After Dilution, Single-Does vial. Mfd

Turkeyfoot Creek Creamery LLC recalls Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton

Turkeyfoot Creek Creamery LLC recalls Turkeyfoot Creek Creamery Mocha Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with

Big O' Smokehouse, Inc. recalls Big O' Smokehouse 4lb Whitefish Spread Big O' Smokehouse 8oz Whitefish Spread Packaged in plastic containers

Turkeyfoot Creek Creamery LLC recalls Turkeyfoot Creek Creamery Cookies and Cream Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper

Turkeyfoot Creek Creamery LLC recalls Turkeyfoot Creek Creamery Cacao Strawberry Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper

Yerba Prima Inc recalls Great Plains Bentonite + Herbal Detox Capsules 60 capsules, packaged in PETE amber bottle, white plastic cap and tamper

Turkeyfoot Creek Creamery LLC recalls Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper

Mightylicious Inc. recalls MIGHTYLICIOUS Vegan Oatmeal Coconut Cookies Gluten-Free, Dairy-Free, Allergen Friendly, Egg-Free, Non-GMO, Kosher,

Turkeyfoot Creek Creamery LLC recalls Turkeyfoot Creek Creamery Chocolate Peanut Butter Artisan Ice Cream, One Pint (473 ml), packaged individually in a

HOFOOD99 INC. recalls Enoki Mushroom in a 200g, green and clear plastic package marked with UPC Barcode 6 976532 310051 on the back label; a

Turkeyfoot Creek Creamery LLC recalls Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with