Practi-0 — Class I drug recall D-0434-2015
Terminated recall by Wallcur Incorporated, reported 2015-04-15, distributed in PR. Non-sterility: Product is made in a non-sterile facility and is not intended for use in humans or animals.
| Recall number | D-0434-2015 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wallcur Incorporated, San Diego, CA, United States |
| Recall initiated | 2015-01-06 |
| Classified | 2015-04-06 |
| Reported by FDA | 2015-04-15 |
| Terminated | 2015-11-25 |
| Distributed | PR |
| Countries outside the US | CA |
| Quantity | 18,657 bags |
| Reason classes | sterility |
| NDC | 05108-0954-71, 05108-0954-72, 05108-0954-73, 05108-0954-74, 05108-0954-75 |
Product
Practi-0.9% Sodium Chloride, 50 mL, 100 mL, 250 mL, 500 mL, and 1000 mL bags, Product of China, Wallcur, San Diego, CA, 92111, USA; Wallcur Practi Products for Clinical Simulation; NDCs 5108-0954-75, 5108-0954-71, 5108-0954-72, 5108-0954-74, 5108-0954-73.
Reason for recall
Non-sterility: Product is made in a non-sterile facility and is not intended for use in humans or animals.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0434-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.