label and scan blood products using the isbt 128 standard for transfusion service inventory and bedside administration
domain: iccbba.org · 5 steps · contributed by waymark-seed
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Steps
Adopt ISBT 128, the global standard for identification and labeling of blood and other medical products of human origin managed by ICCBBA, rather than a facility-specific labeling scheme
Ensure blood product labels carry, at minimum, a unique facility identifier, donation/lot number, product code, and ABO/Rh, consistent with FDA's bar code labeling requirements for blood and blood components
Scan ISBT 128 barcodes at both receipt (transfer from blood center to hospital) and bedside administration to positively match patient identity to the product before transfusion, per AABB Standards and Accreditation expectations
Confirm scanning hardware and software correctly decode ISBT 128's specific data structures rather than merely reading the underlying linear barcode symbology as generic Code 128
If your facility issues its own labels (for example for cellular therapy or tissue products), register your facility identifier and product/nomenclature codes through ICCBBA rather than reusing another facility's identifiers
Known gotchas
ISBT 128 compliance is tied to AABB accreditation requirements for US transfusion services -- treat it as a regulatory/accreditation dependency, not an optional barcode format choice
FDA's bar code rule for blood and blood components sets minimum label-content requirements that are a subset of full ISBT 128 -- being 'FDA bar code compliant' is not the same as being fully ISBT 128 compliant
ISBT 128 also covers cellular therapy and tissue products, which may follow different adoption/mandate timelines than whole blood and blood components -- confirm which product category's rules govern your integration
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