Skip to main content

FDA recall, , Moderate risk

Blood Bank of Hawaii Apheresis Red Blood Cells, Pooled Cryoprecipitated AHF and Red Blood Cells

Apheresis Red Blood Cells, Leukocytes Reduced, collected from a donor who had a hepatitis exposure prior to donation, were distributed.

Recall ended Jun 22, 2026. Still check yours.

What happened

Blood Bank Of Hawaii distributed Red Blood Cells, Leukocytes Reduced, Apheresis Red Blood Cells, Leukocytes Reduced, and Pooled Cryoprecipitated AHF, each collected from a donor who had a hepatitis exposure prior to donation, in Hawaii. The recall began June 20, 2025, and was added to FDA's Enforcement Report on June 22, 2026.

2 photos

What to do

We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:

  1. Check the FDA or company notice for instructions specific to this product.
  2. Ask your pharmacist or doctor whether your lot is affected and what to do.

Is yours affected?

3 products

Compare these details with yours, then check the recall notice to see which units are recalled.

  1. Apheresis Red Blood Cells, Leukocytes Reduced

    Reason: Apheresis Red Blood Cells, Leukocytes Reduced, collected from a donor who had a hepatitis exposure prior to donation, were distributed.

  2. Red Blood Cells, Leukocytes Reduced

    Reason: Red Blood Cells, Leukocytes Reduced, collected from a donor who had a hepatitis exposure prior to donation, were distributed.

  3. Pooled Cryoprecipitated AHF

    Reason: Pooled Cryoprecipitated AHF, collected from a donor who had a hepatitis exposure prior to donation, was distributed.

Recall details

Company began the recall
Company
Blood Bank Of Hawaii
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
99005
Recall numbers
B-0064-2026 to B-0066-2026

All recalls from Blood Bank Of Hawaii

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA · Recall ended

  3. In FDA's weekly enforcement report

  4. Listed on Recall Canary

  5. Archived

Summary by Recall Canary, written with AI · summary updated Oct 24, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)