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FDA recall, , Moderate risk

Suncoast Communities Blood Bank Red Blood Cells and Whole Blood

Red Blood Cells and Whole Blood were distributed from donors with incomplete eligibility screening.

Recall ended Aug 19, 2026. Still check yours.

What happened

Suncoast Communities Blood Bank, Inc. recalled Red Blood Cells and Whole Blood because the products were collected from donors for whom donor eligibility screening was incomplete. The recall began May 6, 2026, and was added to the FDA's Enforcement Report on August 19, 2026. The products were distributed in California and Florida.

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?

2 products

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

  1. Red Blood Cells

    Reason: Red Blood Cells, collected from donors for whom donor eligibility screening was incomplete, were distributed.

  2. Whole Blood

    Reason: Whole Blood, collected from donors for whom donor eligibility screening was incomplete, were distributed.

Recall details

Company began the recall
Company
Suncoast Communities Blood Bank, 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
99412
Recall numbers
B-0181-2026 to B-0182-2026

All recalls from Suncoast Communities Blood Bank, Inc.

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. Listed on Recall Canary

  4. In FDA's weekly enforcement report

  5. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 12, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)