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 10541–10560 of 11714 results

Sort:

Newest first Oldest first

Canon Medical System, USA, INC.: System INFX-8000C

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

FDAFeb 5, 2021Nationwide• Canon Medical System, USA, INC.

Unknown Manufacturer: DJO EMPOWR KNEE Femoral Sizer

Incorrect assembly of a subcomponent by a vendor and as a result, the windows provided to show the size are facing the opposite direction.

FDAFeb 5, 2021FL, IN, MN

Siemens Medical Solutions USA, Inc.: Product Label - ACUSON Sequoia *** Power Input: 100-240V~...

The ultrasound system averages the Mean Sac Diameter (MSD) and Gestational Sac Diameter (GSD) into the Estimated Date of Delivery (EDD) calculation. This may result in an incorrect EDD, which may influence patient management decisions regarding induction of labor and elective caesarean delivery, which may result in premature births.

FDAFeb 4, 2021AL, AK, AZ +41 more• Siemens Medical Solutions USA, Inc.

Siemens Healthcare Diagnostics, Inc.: Dimension Vista HDLC - colorimetric method, lipoproteins ...

Siemens Healthcare Diagnostics Inc. has confirmed the potential for erroneous results due to discolored reagent observed in some wells 5 and 6 of Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent cartridges lot 20062BA.

FDAFeb 3, 2021Nationwide• Siemens Healthcare Diagnostics, Inc.

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF): Implantable cardioverter defibrillators (ICD): 1) Evera f...

A small percentage of implanted cardiac devices, from a well-defined subset, may experience a shortened Recommended Replacement Time (RRT) to End of Service (EOS) interval following an earlier-than-expected RRT observation

FDAFeb 3, 2021Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Enoxaparin Sodium (Apotex) – labeling mixup (2021)

Labeling; Label Mixup; syringe barrels may contain markings for 100 mg/mL (corresponding to 100 mg/mL strength) instead of 150 mg/mL (corresponding to 120 mg/0.8mL strength)

FDAFeb 2, 2021Nationwide• Apotex Corp.

Enoxaparin Sodium (Apotex) – labeling mixup (2021)

Labeling; Label Mixup; syringe barrels may containing markings for 150 mg/mL (corresponding to 120 mg/0.8mL strength) instead of 100 mg/mL markings (corresponding to 100 mg/mL strength)

FDAFeb 2, 2021Nationwide• Apotex Corp.

Bovie Medical Corporation: Velocity Disposable Bipolar Ablators - Product Usage: int...

There can be a potential breach of the sterile packaging barrier due to the development of pinholes at the crease of the double-folded edge of the current package configuration.

FDAFeb 1, 2021Nationwide• Bovie Medical Corporation

Bovie Medical Corporation: HNM Disposable Bipolar Ablators - Product Usage: intended...

There can be a potential breach of the sterile packaging barrier due to the development of pinholes at the crease of the double-folded edge of the current package configuration.

FDAFeb 1, 2021Nationwide• Bovie Medical Corporation

Bovie Medical Corporation: ConMed Disposable Bipolar Ablators - Product Usage: inten...

There can be a potential breach of the sterile packaging barrier due to the development of pinholes at the crease of the double-folded edge of the current package configuration.

FDAFeb 1, 2021Nationwide• Bovie Medical Corporation

Stryker Communications: S-Series Equipment Management System; Model Number(s):068...

The manufacturer has become aware that there is a likelihood that the S-Series Equipment Management System Capacitive Touch Controls on the MFRs rotational electrical magnetic brakes may disengage when an electrocautery device is in use.

FDAJan 29, 2021Nationwide• Stryker Communications

Spironolactone Tablets (Bryant Ranch) – Label Mix-Up (2021)

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg may contain spironolactone 25 mg tablets.

Class IIModerate

FDAJan 27, 2021Nationwide• Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Spironolactone Tablets (Bryant Ranch) – Label Mix-Up (2021)

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.

FDAJan 27, 2021Nationwide• Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Metformin Hydrochloride Tablets (Nostrum) – NDMA Impurity (2021)

CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level.

Class IIModerate

FDAJan 25, 2021Nationwide• Nostrum Laboratories Inc

Boston Scientific Corporation: Captivator Single-Use Polypectomy Snares, Captiflex Singl...

Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.

FDAJan 19, 2021Nationwide• Boston Scientific Corporation

Boston Scientific Corporation: Captivator II Single-Use Polypectomy Snares Outer box U...

Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.

FDAJan 19, 2021Nationwide• Boston Scientific Corporation

ReNovo, Inc.: Various reprocessed products: PROVISION, Reprocessed Smi...

Non-sterile product was shipped to customers labelled as sterile.

FDAJan 19, 2021Nationwide• ReNovo, Inc.

Boston Scientific Corporation: Captivator/Captiflex/Sensation Short Throw Single-Use Pol...

Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.

FDAJan 19, 2021Nationwide• Boston Scientific Corporation

Stryker Sustainability Solutions: Stryker Sustainability Solutions REF HARH36 Ethicon Endo-...

Product was distributed without receiving regulatory clearance.

FDAJan 19, 2021Nationwide• Stryker Sustainability Solutions

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.): CervAlign Anterior Cervical Plate System-Cervalign, 1 Lev...

Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

FDAJan 15, 2021Nationwide• RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

1...526 527528529 530...586

Page 528 of 586Next