FDA recall, , Moderate risk
Terumo BCT Rika Plasma Donation System
The Rika Plasma Donation System has a potential safety issue with an electrical component in a control valve.
Recall ended Jul 15, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
The Rika Plasma Donation System has a potential safety issue with an electrical component within the high-pressure and/or low-pressure control valve. This could cause a safety issue.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Match the model number and UPC listed under your product.
A UPC is the number printed under a barcode.
Rika Plasma Donation System
- Model
- 42000
- UPC
- 0502058342007
Recall details
- Company began the recall
- Sold in
US We have 3 customers, but there are devices at 369 locations. Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, PR, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia
- Company
- Terumo BCT, Inc.
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 97272
- Recall number
- B-0051-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Recall ended
Listed on Recall Canary
Archived
