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 ↗

RSS Feed

Home
/
Brands
/
WINGDERM ELECTRO-OPTICS LTD. Room 312 Building D-3, Dongsheng Science Park, No.66 Of Xixiaokou Road, Haidian District Beijing China

WINGDERM ELECTRO-OPTICS LTD. Room 312 Building D-3, Dongsheng Science Park, No.66 Of Xixiaokou Road, Haidian District Beijing China Recalls

All product recalls associated with WINGDERM ELECTRO-OPTICS LTD. Room 312 Building D-3, Dongsheng Science Park, No.66 Of Xixiaokou Road, Haidian District Beijing China.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

442

Class I (Serious)

138

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 621–640 of 7663 recalls

Diode Laser Hair Removal WLA-01 (WINGDERM) – Labeling Issue (2024)

All model WLA-01 systems sold to US customers are found to have labeling non-compliances

Low

FDAAug 23, 2024Nationwide• WINGDERM ELECTRO-OPTICS LTD. Room 312 Building D-3, Dongsheng Science Park, No.66 Of Xixiaokou Road, Haidian District Beijing China

Non-ablative Laser System WFB-01 (WINGDERM) – Software Bug (2024)

Model WFB-01 sold to US customers before Aug 23, 2022 has been found to have a software bug (6 units). All WFB-01 models sold to US customers found to have labeling non-compliances (22 units)

Low

FDAAug 23, 2024Nationwide• WINGDERM ELECTRO-OPTICS LTD. Room 312 Building D-3, Dongsheng Science Park, No.66 Of Xixiaokou Road, Haidian District Beijing China

MultiDiagnost Eleva (PHILIPS) – Cable Hose Carrier Risk (2024)

Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or bolts) which May Result in Parts Falling and/or Part of the Cable Hose Dropping, and result in injury.

1...30 313233 34...384

Page 32 of 384Next

High

FDAAug 22, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Azurion System (PHILIPS) – Cable Hose Carrier Risk (2024)

Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or bolts) which May Result in Parts Falling and/or Part of the Cable Hose Dropping, and result in injury.

High

FDAAug 22, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

INTEGRIS Allura System (PHILIPS) – Cable Hose Carrier Risk (2024)

Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or bolts) which May Result in Parts Falling and/or Part of the Cable Hose Dropping, and result in injury.

High

FDAAug 22, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Allura Xper OR Table (PHILIPS) – Cable Hose Carrier Risk (2024)

Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or bolts) which May Result in Parts Falling and/or Part of the Cable Hose Dropping, and result in injury.

High

FDAAug 22, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

DeWALT Battery Mowers (Stanley Black & Decker) – Laceration Hazard (2024)

Laceration Risk

This recall involves 2024 model year DeWALT Battery 21" Push walk-behind mowers, model numbers DCMWP234U2 and DCMWP600X2, and DeWALT Battery 21" Self-Propelled walk-behind mowers, model numbers DCMWSP256U2 and DCMWSP650Y2. The mowers are black, gray and yellow and have DeWALT printed in yellow on the front or side of the mower. The model number is printed on the rear door of the mower. A date code formatted as 20XX YY-58, with 20XX for year, YY for week, and 58 as the factory code, is laser-printed in yellow on the left side of the mower, just above the left rear wheel. Only date codes 2023 32-58 through 2024 13-58 are affected. Mowers manufactured after March 2024 (2024 14-58) are not affected.

High

CPSCAug 15, 2024Nationwide• Stanley Black and Decker Inc., of New Britain, Connecticut

Great Value Apple Juice (Refresco) – Arsenic Levels (2024)

Product contains inorganic arsenic above action level set in industry guidance (13.2ppb)

Class IIModerate

FDAAug 15, 2024AL, CT, DE +24 more• Refresco Beverages US Inc

Varithena Injection Pack (Biocompatibles) – Delivery System Defect (2024)

Defective Delivery System: incorrect silicone oil-free NormJect 10 mL Luer Lock Solo syringes packaged in the pack, instead of the required silicone oil-free NormJect 10 mL Luer Solo syringes (luer slip connection).

Class IIILow

FDAAug 15, 2024Nationwide• Biocompatibles UK, Ltd.

Tegaderm CHG (3M) - Foreign Substance Contamination (2024)

Contamination with foreign substance matter

Moderate

FDAAug 14, 2024Nationwide• 3M Company Health Care Business 3m Center

Seer Home EEG System (Seer Medical) - EMC Assessment Gap (2024)

During CAPA investigations of sight production inconsistencies, it was highlighted that previous Electromagnetic Compatibility (EMC) assessments related to RF radiated emissions may not be reasonably equivalent to the current product due to design changes in the system. A new CAPA was opened to investigate the radiated emissions compliance issues. - Seer Home Systems distributed and retained in the field were not compliant with Electromagnetic Compatibility (EMC) testing according to IEC 60601-1-2 - Seer Home Systems, including accessories, were manufactured and distributed without application of proper design change and manufacturing controls - Seer Home Systems were distributed with labeling deficiencies

High

FDAAug 12, 2024Nationwide• SEER MEDICAL PTY LTD 278-284 Queensberry St Melbourne Australia

BD FACSDuet Preparation System (BD) - Sample Dispensing Error (2024)

Sample preparation system with software may cause: 1) Multidispense feature enabled with 2-tube assay: Specimen volume dispensed into tube1 at least 3% higher than volume in tube2, or 2) Absolute counts calculated using Trucount Tubes: increased volume in tube1 may result in 20% higher absolute counts in tube 1 than tube 2; could result in additional blood collection, delayed results/patient therapy.

Moderate

FDAAug 12, 2024AK, CA, ID +10 more• Becton, Dickinson and Company, BD Bio Sciences

Mercedes-Benz AMG GLB35 (Mercedes-Benz) - Brake Hose Routing Issue (2024)

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2024 AMG GLB 35 4MATIC vehicles. The brake hoses on the rear axle may have been improperly routed, which could allow chafing, and result in a brake fluid leak.

High

NHTSAAug 9, 2024Nationwide• MERCEDES-BENZ

GE Giraffe Warmer (GE HealthCare) - Electrical Safety Gap (2024)

GE HealthCare has become aware that complete electrical safety testing was not conducted during manufacturing of certain Giraffe and Panda iRes Warmers. There are multiple electrical safety protections included in the product design. However, because the electrical safety testing in manufacturing was incomplete for these devices, there is the potential for leakage current to exceed IEC 60601 limits.

High

FDAAug 9, 2024Nationwide• Wipro GE Healthcare Private Ltd. 122 Part 1 Odyssey And Galileo Bengaluru India

GE Panda iRES Warmer (GE HealthCare) - Electrical Safety Gap (2024)

High

FDAAug 9, 2024Nationwide• Wipro GE Healthcare Private Ltd. 122 Part 1 Odyssey And Galileo Bengaluru India

ViewPoint Imaging System (GE Healthcare) - Cybersecurity Vulnerability (2024)

The National Institute of Standards and Technology (NIST) has identified in the National Vulnerability Database (NVD) that NexGen Healthcare Mirth Connect, prior to version 4.4.1, has a potential vulnerability allowing the deserialization of untrusted data (CVE-2023-43208). Mirth products may have been installed and configured with your ViewPoint / ViewPoint 6 system by GE HealthCare. This vulnerability could allow a malicious actor to access the system and potentially manipulate patient data.

High

FDAAug 8, 2024Nationwide• GE Healthcare GmbH Oskar-Schlemmer-Str. 11 Munich Germany

Philips Allura Xper System (Philips) - Bolt Placement Error (2024)

A half-threaded bolt was included in the LTE kits instead of the correct full-threaded bolt.

Moderate

FDAAug 8, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Finger-Ease Guitar Lubricants (Chem-Pak) – Skin Irritation (2024)

This recall involves one production batch of Finger-Ease Guitar String Lubricant. The product is a clear aerosol spray sold in a white-color steel can with a black cap. The product measures about 1.5 inches long, 1.5 inches wide and 6 inches tall, and weighs about 4.5 ounces. The product has a picture of a brown guitar with the words "Tone Finger Ease Guitar String Lubricant" in brown, black and red lettering. There is a red horizontal stripe on the can. Printed on the can is "Manufactured by Chem-Pak, Inc.", and the production batch code is printed in black ink on the bottom of the steel container with model number 220B and lot code 106824.

Moderate

CPSCAug 8, 2024Nationwide• Chem-Pak Inc., of Martinsburg, West Virginia

ViewPoint 6 System (GE Healthcare) - Cybersecurity Vulnerability (2024)

High

FDAAug 8, 2024Nationwide• GE Healthcare GmbH Oskar-Schlemmer-Str. 11 Munich Germany

Biodesign Inguinal Hernia Graft C-IHM-10X15 (Cook Biotech) – Early Expiration (2024)

Products expire prior to the expiration date printed on the product labeling

Moderate

FDAAug 7, 2024Nationwide• Cook Biotech, Inc.