Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

Search Product Recalls

Try:····

Filters

Category

All Categories Food Medication Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Time Period

All Time Last 30 Days Last 90 Days Last Year

State

Severity

All Severities Class I (High Risk)Class II (Moderate)Class III (Low)

Source

All Sources FDA CPSC USDA NHTSA

Status

Include terminated recalls

Clear all filters

Showing 2521–2540 of 4940 results

Sort:

Newest first Oldest first

X5-1 Transducer Probe (Philips) – Useful Life Clarification (2025)

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

FDAJul 3, 2025Nationwide• Philips Ultrasound, Inc

Orascoptic Superior Visualization (Orascoptic) – Nickel Allergy Risk (2025)

Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.

FDAJul 3, 2025Nationwide• Orascoptic Surgical Acuity

Evergreen Farm Korean Pear Juice – Sanitation Concern (2025)

Lack of pasteurization and sanitation records

Class IIModerate

FDAJul 3, 2025NJ, NY, PA• Evergreen Orchard Farm, LLC

Autocar Xpeditor (Autocar) – Air Tank Deficiency (2025)

Autocar, LLC (Autocar) is recalling certain 2015-2022 ACTT (Xspotter) and ACX (Xpeditor) vehicles. The air tanks have an insufficient volume of air for the brake system. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems."

NHTSAJul 3, 2025Nationwide• AUTOCAR

Evergreen Farm Jujube Juice – Sanitation Concern (2025)

Lack of pasteurization and sanitation records

Class IIModerate

FDAJul 3, 2025NJ, NY, PA• Evergreen Orchard Farm, LLC

Stryker SmartPump Tourniquet (Stryker) – Cuff Detachment Risk (2025)

Tourniquet cuff flange may become detached from the bladder. If leak occurs during the procedure, there may be risk of hemorrhage, resulting in blood loss greater than expected. Other serious risks include cerebral hypotension and cardiovascular collapse and arrest, risking stroke or death. Specific to IVRA, patient toxicity may also occur due to rapid systemic absorption of anesthetics.

FDAJul 2, 2025Nationwide• Stryker Corporation

GE OEC 9800 (GE Medical Systems) – Regulatory Non-Conformance (2025)

GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.

FDAJul 2, 2025Nationwide• GE Medical Systems, LLC

POLESTAR 2 (POLESTAR) – Service Brake Issue (2025)

Polestar Automotive USA, Inc. (Polestar) is recalling certain 2021 and 2024 Polestar 2 vehicles. In certain driving scenarios while coasting down a hill and using "One Pedal Drive," the vehicle may lose brake function.

NHTSAJul 2, 2025Nationwide• POLESTAR

BLUE ARC BA4L-800 (BLUE ARC) – Brake Caliper Spacer (2025)

Shyft Group (Shyft) is recalling certain 2024-2025 Blue ARC BA4L-800 vehicles. The spacer for the brake caliper may be too big, resulting in an increased air gap.

NHTSAJul 2, 2025Nationwide• BLUE ARC

Sparrow Ascent Patient Controller (Spark Biomedical) – Cable Disconnect (2025)

Due to manufacturing issue, neurostimulator device may experience "cable disconnect" error message and interruption to stimulation output.

FDAJul 2, 2025Nationwide• Spark Biomedical Inc

Artisan Style 1/2 Loaf (Lewis Bakeries) – Undeclared Hazelnut (2025)

Undeclared Allergen

Undeclared allergen: Hazelnut due to mispackaging. Product with hazelnuts was put in the Artisan Style 1/2 loaf bags. Bags do not have allergen statement that includes hazelnuts.

Class IIModerate

FDAJul 2, 2025AR, FL, IL +8 more• LEWIS BAKERIES

Activated Almonds (SunBiotics) – Salmonella Contamination (2025)

Salmonella Contamination. Firm detected salmonella on one batch of our SunBiotics Oat Milk Chocolate Covered Almonds.

FDAJul 2, 2025AK, CA, CO +4 more• WINDY CITY ORGANICS LLC

Smoked Gouda (Boar's Head) – Mislabeling (2025)

Mislabeling

FDAJul 2, 2025FL• Alpine Slicing and Cheese Conversion Company

Amlodipine Benazepril Capsules (Lupin) – Incorrect Expiration (2025)

Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027

Class IIModerate

FDAJul 2, 2025Nationwide• Lupin Pharmaceuticals Inc.

GE OEC 9900 Elite C-arm Systems (GE Medical Systems) – Non-Conformance (2025)

GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.

FDAJul 2, 2025Nationwide• GE Medical Systems, LLC

Robotic/Laparoscopy Kit (Carefree Surgical) – Sterility Compromise (2025)

Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging

FDAJul 1, 2025Nationwide• Carefree Surgical Specialties

Junctional Emergency Treatment Tool (North American Rescue) – Manufacturing Defect (2025)

Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use.

FDAJul 1, 2025Nationwide• North American Rescue LLC.

Peripheral Parenteral Nutrition (CAPS) – Processing Controls (2025)

Lack of Processing Controls; prescriptions were compounded in an ISO-5 area where it was identified that a daily cleaning step was not sufficiently documented.

Class IIModerate

FDAJul 1, 2025CA• Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles

Ingenia 3.0T CX (Philips) – Gradient Coil Failure (2025)

The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.

FDAJun 30, 2025Nationwide• Philips North America

MR 7700 (Philips) – Gradient Coil Failure (2025)

The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.

FDAJun 30, 2025Nationwide• Philips North America

1...125 126127128 129...247

Page 127 of 247Next