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 4801–4820 of 22534 results

Sort:

Newest first Oldest first

Neodent Healing Abutment (Preat) – Dimensional Gap Risk (2023)

The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage

FDAJul 18, 2023CA, FL, NJ +4 more• Preat Corp

Neodent Healing Abutment (Preat) – Dimensional Gap Risk (2023)

The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage

FDAJul 18, 2023CA, FL, NJ +4 more• Preat Corp

RayCare Software (RaySearch) – Allergy Warning Issue (2023)

An issue was found in Software RayCare 5A, 5B, 6A, including service packs, where an allergy warning against medication substance (drug ingredient) will not be displayed as expected under certain circumstances

High

FDAJul 17, 2023Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Aquilex Fluid System (WOM) – Volume Display Limit (2023)

The display of inflow volume can reach its limit of 30,000 ml during long procdeure and the inflow volume display will freeze at the maximum value while the deficit will start counting backwards until 0 ml is reached and may result in fluid overload

FDAJul 17, 2023Nationwide• WOM World Of Medicine AG Alte Poststr. 11 Ludwigsstadt Germany

L-Aneurysm Clip (Peter Lazic) – Incorrect Color (2023)

Wrong product coloring. The paddle clips should be blank, but they are colored blue.

FDAJul 14, 2023Nationwide• Peter Lazic Gmbh Immelmannweg 2 Tuttlingen Germany

Copan Transfer Pipette (Copan) – Aspiration Defect (2023)

Due to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance

FDAJul 14, 2023CA• Copan Diagnostics Inc

Q2 Multiport Extension Set (Quest Medical) – Administration System (2023)

For administration of intravenous fluids to a patient s vascular system utilizing needle-free components and I.V. manifold for multiple simultaneous intravenous therapy via gravity, syringe, or infusion pump. Use of a needle-free system may aid in the prevention of needle-stick injuries.

FDAJul 14, 2023AL, CA, CO +16 more• Quest Medical, Inc.

MobileLink Acetabular Cup (Waldemar Link) – Incorrect Offset (2023)

Product is labeled with incorrect offset.

FDAJul 14, 2023AL, NV, NJ• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Snowden-Pencer MIS Grasper (Carefusion) – Rotation Knob Defect (2023)

Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.

FDAJul 13, 2023Nationwide• Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845

ACUSON Redwood Ultrasound (Siemens) – Preset Compatibility Problem (2023)

If a user-generated preset for an 18L6 transducer created on a 1.0 ultrasound system is used with a 2.0 ultrasound system, the 2.0 ultrasound system will display underestimated measurement results when using an 18L6 transducer and viewing in the Dual format visualization function, which may lead to misdiagnosis of a patient's condition or influence patient management decisions in a negative way.

FDAJul 13, 2023Nationwide• Siemens Medical Solutions USA, Inc.

ACL TOP Family Analyzer (Instrumentation Lab) – Result Misidentification (2023)

Sample misidentification could occur under specific conditions and patient management altered based on an incorrectly assigned result

FDAJul 13, 2023Nationwide• Instrumentation Laboratory

Embrace2 Device (Empatica) – Battery Life Limitation (2023)

May have a battery life lasting less than the full 48 hours, requiring the device to be charged more frequently.

FDAJul 13, 2023Nationwide• EMPATICA SRL Via Enrico Stendhal

Plum 360 Infusion System (ICU Medical) – Alarm Signal Issue (2023)

Due to a manufacturing defect of a supplier provided component, there is a potential that the audible signal for an alarm may not sound under certain conditions.

FDAJul 13, 2023Nationwide• ICU Medical Inc

Chevalier Valvulotome (LeMaitre) – Cutter Surface Defect (2023)

Laceration Risk

Burrs (molding flash) on the cutter may tear the harvested vien

FDAJul 13, 2023Nationwide• LeMaitre Vascular, Inc.

IMPIX 3D (Medicrea) – Packaging Pinhole Issue (2023)

There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.

FDAJul 12, 2023Nationwide• Medicrea International Vancia Vancia Rillieux La Pape France

IMPIX MANTA (Medicrea) – Packaging Pinhole Issue (2023)

There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.

FDAJul 12, 2023Nationwide• Medicrea International Vancia Vancia Rillieux La Pape France

PASS LP (Medicrea) – Packaging Pinhole Issue (2023)

There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.

FDAJul 12, 2023Nationwide• Medicrea International Vancia Vancia Rillieux La Pape France

nanoDot D2DNS (Unknown) – Accuracy Range Issue (2023)

LANDAUER received reports indicating that some nanoDots may potentially be outside of the specified range of +/-5.5% accuracy. Investigation of nanoDots indicated the presence of a potential non-conformance in the Optical Stimulated Luminescence (OSL) material that is beamed after exposure and emits fluorescence proportional to radiation exposure.

FDAJul 12, 2023Nationwide

nanoDot D2DXS (Unknown) – Accuracy Range Issue (2023)

LANDAUER received reports indicating that some nanoDots may potentially be outside of the specified range of +/-5.5% accuracy. Investigation of nanoDots indicated the presence of a potential non-conformance in the Optical Stimulated Luminescence (OSL) material that is beamed after exposure and emits fluorescence proportional to radiation exposure.

FDAJul 12, 2023Nationwide

nanoDot D2DNS Calibrate (Unknown) – Accuracy Range Issue (2023)

LANDAUER received reports indicating that some nanoDots may potentially be outside of the specified range of +/-5.5% accuracy. Investigation of nanoDots indicated the presence of a potential non-conformance in the Optical Stimulated Luminescence (OSL) material that is beamed after exposure and emits fluorescence proportional to radiation exposure.

FDAJul 12, 2023Nationwide

1...239 240241242 243...1127

Page 241 of 1127Next