Quick answers
- Does CPDA-1 blood bag collection system have a boxed warning?
- No. None of the 3 FDA labels we found for this medicine has a boxed warning.
- Is there a shortage of CPDA-1 blood bag collection system?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has CPDA-1 blood bag collection system been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes CPDA-1 blood bag collection system?
- 1 company lists prescription products of CPDA-1 blood bag collection system in the FDA NDC Directory, including GVS TM Inc.
What CPDA-1 blood bag collection system is used for
We did not find an “Indications and Usage” section in the FDA labels for this medicine. See the label on DailyMed →
This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Boxed warning
A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.
The label quoted above has no boxed warning.
0 of 3 FDA labels for this medicine have a boxed warning.
Forms and how it is given
| Dosage forms | Solution |
|---|---|
| Route | Intravenous |
| Prescription products | 2 in the FDA NDC Directory |
| Brand names | Leukotrap Wb System |
Companies that list this medicine
Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.
- GVS TM Inc3 products
FDA approval history
No Drugs@FDA application is linked to these products.
Shortage status
The FDA drug shortage list does not show these products.
Recalls
No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.
Official identifiers
| SPL set ID of the quoted label | 54fddca1-b40c-7af0-e063-6294a90a410e |
|---|---|
| FDA labels (SPL) | 3 |
| Active ingredients (FDA) | ADENINE / CITRIC ACID MONOHYDRATE / DEXTROSE MONOHYDRATE / SODIUM CITRATE / SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE |
Next steps
- Find a pharmacy near youAsk which price applies to you and whether your product is affected by a recall
- Latest FDA drug recallsAll medicines, newest first
- GVS TM IncMaker or distributor
- All prescription drugs A to ZSearch by generic, brand or Spanish name
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Leukotrap WB System, Gvs Tm Inc, effective June 24, 2026; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →