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
/
Richin Trading Inc

Richin Trading Inc Recalls

All product recalls associated with Richin Trading Inc.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

Most Recent

Jan 2026

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 3921–3940 of 21320 recalls

Sun Wave Brand Jelly Cup (Richin Trading) – choking risk (2023)

Choking Hazard

Potential choking hazard

Class IHigh

FDAJun 9, 2023AZ, CA, CO +15 more• Richin Trading Inc

Sun Wave Brand Jelly Cup (Richin Trading) – choking risk (2023)

Choking Hazard

Potential choking hazard

Class IHigh

FDAJun 9, 2023AZ, CA, CO +15 more• Richin Trading Inc

Pearl Milling Self-Rising Corn Meal Mix (PepsiCo) – undeclared milk (2023)

Undeclared Milk

May contain trace amounts of undeclared milk

1...195 196197198 199...1066

Page 197 of 1066Next

Class II

Moderate

FDAJun 9, 2023AL, AZ, AR +24 more• PepsiCo Beverages & Foods

EVIS EXERA III Bronchovideoscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Moderate

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

Bronchovideoscope BF Type (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Moderate

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

Option Elite Retrievable Filter (Argon Medical) – Potential Embolism Risk (2023)

There is the potential that the vena Cava Filter may not perform as intended which may result in pulmonary embolism.

Moderate

FDAJun 8, 2023Nationwide• Argon Medical Devices, Inc

EVIS EXERA Bronchovideoscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Moderate

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

EVIS EXERA II Bronchovideoscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Moderate

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

Bronchovideoscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Moderate

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

Arctic Cat 8000 Snowmobiles (Textron) – fire hazard (2023)

Fire/Burn Risk

This recall involves Textron Specialized Vehicles Arctic Cat 8000 Series Snowmobiles. The snowmobiles were sold in various colors and have "ARCTIC CAT" and the model number printed on each side of the engine cowling. The Vehicle Identification Number (VIN) is located on the front right-hand frame tube beside the right-hand shock.

High

CPSCJun 8, 2023Nationwide• Textron Specialized Vehicles, of Augusta, Georgia

BD Synapsys Informatics Solution (Becton Dickinson) – Patient Data Mis-association (2023)

There is a risk of mis-association of patient demographic data for users who choose to report results manually when their Service Control Unit (SCU) is operating near capacity and are using save actions (Skip, Final Discard, Mark as Read, Save) to process patient results rapidly.

Moderate

FDAJun 8, 2023CA, CO, IL +12 more• Becton Dickinson & Co.

Bronchofiberscope BF Type (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Moderate

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

HF Resection Electrodes (Olympus) – Wire Breakage Caution (2023)

Additional Caution statements in IFU: (1) Due to complaints where the loop wire at the distal end of the HF resection electrode broke after getting in contact with metal objects, such as other endoscopic equipment, implants or stents. As a result, fragments can fall inside the patient and must be retrieved. (2) The second Caution refers to the risk of sparkover when getting in contact with metal parts as this can cause uncontrolled heating of the HF-resection electrode and may result in damage and breakage to the HF-resection electrode tip

High

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

OES Bronchofiberscope (Olympus) – Endobronchial Combustion Risk (2023)

There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

Moderate

FDAJun 8, 2023Nationwide• Olympus Corporation of the Americas

Churritos Corn Flour Sticks (Botanas) – undeclared sesame (2023)

The product labels include a Contains statement that did not disclose sesame for the product that contains sesame. Sesame is included Ingredient statement.

Class IIModerate

FDAJun 8, 2023CA, IN, OR• Botanas Michoacanas

FRED Flow Re-Direction Endoluminal Device (MICROVENTION) – Incorrect Inner Stent Length (2023)

Intracranial aneurysm flow diverter device may be manufactured with an incorrect inner stent length and may not perform as intended.

Moderate

FDAJun 7, 2023Nationwide• MICROVENTION INC.

Vanta AdaptiveStim Neurostimulator (Medtronic) – Cardioversion Damage (2023)

A cardioversion procedure may damage the electronics in the Vanta INS device, making the INS unresponsive and non-functional. As of April 19, 2023, Medtronic has received a total of two complaints concerning this issue from patients implanted with a Vanta INS, both of which have resulted in explant procedures.

Moderate

FDAJun 6, 2023Nationwide• Medtronic Neuromodulation

OmniTom X-ray CT System (NeuroLogica) – Device Mobility Risks (2023)

1. Wheels loosening over time with use of the device could lead to the inability to effectively drive the device and could lead to delay in patient treatment. 2.Batteries used to power the NL5000 device contain contaminated boards, which may impact the ability to power on the device, this could lead to delay for patient treatment

Moderate

FDAJun 6, 2023Nationwide• NeuroLogica Corporation

Catalyft LS Interbody System (Medtronic) – Geometry Specification Issue (2023)

There is the potential for out of specification device geometries. widths, lengths, heights, and lordotic angles to accommodate patient anatomy. These devices can be inserted between two lumbar or lumbosacral vertebral bodies to give support and correction during lumbar interbody fusion surgeries. Implants have a central cavity that allows them to be packed with autogenous bone graft and/or allograft bone graft comprised of cancellous and/or Corticocancellous bone, and/or demineralized allograft bone with bone marrow aspirate.

Moderate

FDAJun 6, 2023Nationwide• Medtronic Sofamor Danek USA Inc

Cios Select X-ray System (Siemens) – Plexiglass Cover Issue (2023)

Incorrect glue was applied on the plexiglass sheet on the single tank cover assembly could potentially fall off and the ingress of liquid may occur, the risk of electric shock exists (e.g., ingress of a large amount of liquid following the plexiglass dropping off, at the same time the user or operator happens to touch the liquid on the cover which is connected to the internal live parts).

High

FDAJun 5, 2023Nationwide• Siemens Medical Solutions USA, Inc