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FDA recall, , Moderate risk

American National Red Cross Red Blood Cells and PF24 Plasma

American National Red Cross Red Blood Cells and PF24 Plasma, collected in a manner that compromises the sterility of the collection system, were distributed.

Recall ended Sep 16, 2026. Still check yours.

What happened

The American National Red Cross recalled PF24 Plasma, Red Blood Cells, Leukocytes Reduced, and Red Blood Cells, Leukocytes Reduced, Irradiated, because they were collected in a manner that compromises the sterility of the collection system. The recall began August 15, 2025, and the FDA added it to its Enforcement Report on September 16, 2026. The products were distributed in New York and Pennsylvania.

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. Red Blood Cells, Leukocytes Reduced

    Reason: Red Blood Cells, Leukocytes Reduced, collected in a manner that compromises the sterility of the collection system, were distributed.

  2. PF24 Plasma

    Reason: PF24 Plasma, collected in a manner that compromises the sterility of the collection system, were distributed.

  3. Red Blood Cells, Leukocytes Reduced, Irradiated

    Reason: Red Blood Cells, Leukocytes Reduced, Irradiated, collected in a manner that compromises the sterility of the collection system, were distributed.

Recall details

Company began the recall
Company
American National Red Cross (the)
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
99598
Recall numbers
B-0177-2026 to B-0179-2026

All recalls from American National Red Cross (the)

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

Summary by Recall Canary, written with AI · summary updated Oct 23, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)