Releasing and storing components
16 min
- Verify donor testing and traceability before releasing a component
- Store and transport each component at its labeled temperature and agitation
- Determine component expiration after processing or system entry
- Calculate red-cell processing recovery from volume and hematocrit
Try first
Get the idea
Release needs the whole record
A collected unit stays in quarantine until its record is complete. Routine release needs every required infectious-disease result, confirmed ABO and D types, and a final label that links the component to its donation.1 The ISBT 128 Donation Identification Number (DIN) is unique to one donation and follows it onto every sample, component and record.2 A repeatedly reactive, unresolved or missing result keeps the donation and every component made from it linked and in quarantine. A final label can be printed while a test is still pending, so release is checked against the record.1,3
Each component has its own conditions
| Component | Storage | Dating |
|---|---|---|
| Red cells | 1–6 °C, transported at 1–10 °C | Set by the anticoagulant and additive, 42 days with AS-1, AS-3, AS-5 or AS-7 |
| Platelets | 20–24 °C with continuous gentle agitation | 5 days, up to 7 with an approved bacterial-risk strategy |
| Granulocytes | 20–24 °C without agitation | 24 hours after collection |
| Frozen plasma and cryoprecipitate | −18 °C or colder | 1 year |
Cold-stored platelets are a separate labeled product with their own preparation, dating and use.3,5 A component found outside its labeled conditions is quarantined and dispositioned under the facility's procedure.4
Opening a system shortens the dating
A sealed collection set is a closed system. Opening it generally limits the component to 24 hours at 1 to 6 °C or 4 hours at 20 to 24 °C. The component then expires at the new limit or its existing expiration, whichever comes first.3 Thawed Fresh Frozen Plasma stored at 1 to 6 °C expires in 24 hours. Thawed cryoprecipitate expires in 6 hours. A pool made in an open system expires 4 hours after entry and never later than the original post-thaw time.3
Processing recovery
Deglycerolization and washing replace supernatant, so the suspension volume can stay close to its starting value as red cells are lost. Recovery therefore compares red-cell volumes. Red-cell volume (mL) = suspension volume (mL) × hematocrit (L/L). Processing recovery (%) = postprocessing red-cell volume ÷ preprocessing red-cell volume × 100. Processing recovery counts the cells retained through processing. The 24-hour posttransfusion recovery is a different measurement, made in the recipient. Recovery is one of several product specifications reviewed before release.4
References
- Electronic Code of Federal Regulations. Title 21, §§606.121, 606.122, 610.40, 610.41, 610.53, 640.5, and 640.25. Accessed September 27, 2026. https://www.ecfr.gov/current/title-21/chapter-I/subchapter-F
- International Council for Commonality in Blood Banking Automation. ISBT 128 Standard Technical Specification. Version 6.2.2. April 2023. Accessed September 27, 2026.
- Association for the Advancement of Blood & Biotherapies. Circular of Information for the Use of Human Blood and Blood Components. June 2024. Accessed September 27, 2026.
- Bloch EM, Campbell-Lee S, McKenna DH Jr, Montemayor-Garcia C, Schwartz J, Shaz B, Storry J, eds. Technical Manual. 22nd ed. AABB; 2026.
- US Food and Drug Administration. Bacterial Risk Control Strategies for Blood Collection Establishments and Transfusion Services to Enhance the Safety and Availability of Platelets for Transfusion: Guidance for Industry. December 2020. Accessed September 27, 2026.
Watch one
A frozen red-cell unit is deglycerolized. Before processing it measures 310 mL at a hematocrit of 0.72 L/L. The final suspension measures 290 mL at a hematocrit of 0.62 L/L.
What is the processing recovery?
- Red-cell volume before = 310 mL × 0.72 = 223.2 mL.
Hematocrit is a volume fraction, so suspension volume times hematocrit gives red-cell volume.
- Red-cell volume after = 290 mL × 0.62 = 179.8 mL.
The final suspension gets the same treatment with its own hematocrit.
- Recovery = 179.8 mL ÷ 223.2 mL × 100 = 80.555…%, reported as 80.6%.
Recovery counts the red cells kept through processing.
- Check against the shortcut: 290 ÷ 310 × 100 = 93.5% would overstate recovery by about 13 percentage points.
Processing replaces supernatant, so suspension volumes hide the red-cell loss.
- Compare 80.6% with the product's recovery specification, then review the rest of the processing record before release.
Recovery is one specification among several.
Your turn
Use it
- 06:30 on September 27, the start of the day shift at the transfusion service.
- An apheresis platelet unit labeled for 20 to 24 °C with agitation sits on a shelf of the 1 to 6 °C red-cell refrigerator. The refrigerator log shows it went in at 23:10.
- A cooler of red cells arrives from the blood supplier. Its validated transport range is 1 to 10 °C, and the arrival reading is 7 °C.
- At 14:00 a red-cell unit with 18 days of dating left is entered for washing in an open system. It goes into the 1 to 6 °C refrigerator.
The clue that settled each decision is the condition written on the label. The platelets left theirs overnight, the red cells in the cooler stayed within their transport range, and the washing wrote a new, earlier expiration onto the red cells.
Results
- Verify donor testing and traceability before releasing a component
- Store and transport each component at its labeled temperature and agitation
- Determine component expiration after processing or system entry
- Calculate red-cell processing recovery from volume and hematocrit
To review
6 questions from this step will come back in Review.
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The rest of this step
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