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 cautionMedical device
Dexcom, Inc. recalls Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog
Dexcom recalls G7 CGM watchOS app versions 2.9.0-2.11.2 for potential glucose data delays that could cause missed hypoglycemic events. Affected users should check their app version and contact Dexcom.
DexcomApr 14, 2026
✓ Lower riskMedical device
Philips North America recalls Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Number (REF): 781377. 3. Model
Philips recalls Ingenia 3.0T MRI scanners with MR Elastography (MRE) that may display incorrect stiffness values due to image reconstruction settings.
PhilipsApr 14, 2026
✓ Lower riskMedical device
Philips North America recalls Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number
Philips recalls SmartPath to Ingenia Elition X with MR Elastography (MRE) models 782118, 782144, and 782163 due to potential stiffness value errors in image reconstruction, which may lead to inaccurate scan results.
PhilipsApr 14, 2026
✓ Lower riskMedical device
Philips North America recalls Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.
Philips recalls SmartPath to dStream 3.0T with MR Elastography (MRE) model 782145 due to potential stiffness value errors from image reconstruction settings. Affected units may display incorrect voxel sizes in scans.
PhilipsApr 14, 2026

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

Latest recalls

Dexcom, Inc. recalls Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog

Philips North America recalls Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Number (REF): 781377. 3. Model

Philips North America recalls Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number

Philips North America recalls Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.

Premier Dental Products Co recalls Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles, Rx only, Manufacturer: Premier Medical Products, 1710

LACTALIS CANADA, INC recalls Specially SELECTED brand Vanilla Creme Brulee; NET WT 3.6oz (103g); INGREDIENTS: CREAM (MILK, CREAM), FROZEN YOLK MIX

HARLEY-DAVIDSON FLHC (2025) recall — Service Brakes, Hydraulic

Jolife AB recalls LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model

O&M HALYARD INC recalls Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.),

HF Acquisition Co LLC recalls Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12

HF Acquisition Co LLC recalls Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52

Physio-Control, Inc. recalls LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219,

Unichem Pharmaceuticals USA Inc. recalls busPIRone Hydrochloride Tablets, USP, 5 mg, 500-count bottle, Rx Only, Manufactured by Unichem Laboratories LTD., Ind,

Raja Foods and Vegetables Inc. recalls Swad Orange Flavored Masala Candy

Guangdong Zonegoing Food Co., LTD recalls 52USA brand POPPING BOBA; STRAWBERRY FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food

Guangdong Zonegoing Food Co., LTD recalls 52USA brand POPPING BOBA; MANGO FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food

Guangdong Zonegoing Food Co., LTD recalls 52USA brand POPPING BOBA; PASSION FRUIT FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food

Raja Foods and Vegetables Inc. recalls Swad Mango Flavored Masala Candy

Stryker Sustainability Solutions recalls BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Stryker Sustainability Solutions recalls BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Stryker Sustainability Solutions recalls CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Stryker Sustainability Solutions recalls BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Integra LifeSciences Corp. (NeuroSciences) recalls Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Stryker Sustainability Solutions recalls BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER