Drug recall
Anticoagulant Sodium Citrate 4% w/v Solution USP, 250 mL VIAFLEX Plastic Container Product Code 2B7867Q NDC…
FDA recall event 99715 · Class I · Baxter Healthcare Corporation
Key facts
| Event ID | 99715 |
|---|---|
| Recall numbers | B-0001-2027 |
| Recalling firm | Baxter Healthcare Corporation |
| Product type | Biologics |
| Products | Anticoagulant Sodium Citrate 4% w/v Solution USP, 250 mL VIAFLEX Plastic Container Product Code 2B7867Q NDC 0338-9669-01 Strength per dose, dosage: 250mL, Each 100mL contains 4 g Sodium Citrate, USP… |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Baxter International Inc. is voluntarily recalling one lot of Anticoagulant Sodium Citrate Solution (Lot # Y493475) due to the potential presence of particulate matter identified as fiberglass in the… |
| Initiation date | Aug 19, 2026 |
| Report date | Oct 7, 2026 |
| City | Deerfield |
| State | IL |
| Country | United States |
| FEI number | 1417572 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: