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
/
MICHIGAN HERBAL REMEDIES

MICHIGAN HERBAL REMEDIES Recalls

All product recalls associated with MICHIGAN HERBAL REMEDIES.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

198

Class I (Serious)

410

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 1481–1500 of 3552 recalls

Pathway Hemp Oil Drops (Michigan Herbal) – Lead contamination (2020)

Undeclared Allergen

Chemical contamination: product contains elevated levels of undeclared lead.

Class IHigh

FDAJun 18, 2020Nationwide• MICHIGAN HERBAL REMEDIES

LoFric Origo Catheter (Wellspect) – Potential Product Defect (2020)

Wellspect Healthcare is voluntarily recalling certain LoFric Origo" urethral catheters due to a potential defect which may be present in the catheter s distal tip.

FDAJun 17, 2020AL, AZ, CA +19 more• Wellspect HealthCare (Division of DENTSPLY IH AB) Aminogatan 1 Molndal Sweden

DxA 5000 (Beckman Coulter) – Sample ID Confusion (2020)

The DxA 5000 instructions for use may be confusing regarding the re-use of sample IDs. Beckman Coulter has received complaints where the re-use of sample barcodes were not being detected by the system .

1...73 747576 77...178

Page 75 of 178Next

FDAJun 17, 2020Nationwide• Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munich Germany

LoFric Origo Tiemann Catheter (Wellspect) – Potential Product Defect (2020)

Wellspect Healthcare is voluntarily recalling certain LoFric Origo" urethral catheters due to a potential defect which may be present in the catheters distal tip.

The tubes may have been delivered to some users without labels. Users may not be able to identify the tubes without these labels. If samples stored or transported in tubes are tested on certain systems or come into contact with bleach they can produce cyanide gas. The solution in these tubes contains guanidine thiocynate and may put laboratory personnel at risk of exposure to cyanide gas when it comes into contact with bleach or reagents containing bleach.

FDAJun 3, 2020Nationwide• LONGHORN VACCINES AND DIAGNOSTIC 2 Bethesda Metro Cente

ANAX Poly-Reduction Screw (U & I Corp) – laser etching error (2020)

6.0x50mm poly-reduction screws were laser etched 6.0x45

FDAMay 26, 2020AZ• U & I CORP. 20 Sandan-Ro 76 Beon-Gil Uijeongbu Korea (the Republic of)

RayStation Software (RaySearch) – data import issue (2020)

It is not obvious that the manual import of a treatment record into RayCare PACS does not automatically import the same data into RayTreat. In addition, there is an issue found with the display of planned and recorded Gantry Angle in the delivered beam list in RayTreat.

FDAMay 26, 2020IN• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden