Marketing brochures for the PowerPICC and PowerPICC SOLO catheters — Class II medical device recall Z-2808-2015
Terminated recall by Bard Access Systems, reported 2015-09-30. Bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to
| Recall number | Z-2808-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bard Access Systems, Salt Lake City, UT, United States |
| Recall initiated | 2015-07-20 |
| Classified | 2015-09-23 |
| Reported by FDA | 2015-09-30 |
| Terminated | 2017-02-10 |
| Quantity | 1,811 |
Product
Marketing brochures for the PowerPICC and PowerPICC SOLO catheters
Reason for recall
Bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to incorrect indication for use contained in the brochure.
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/Z-2808-2015. 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.