FDA Device recall Z-2808-2015
Marketing brochures for the PowerPICC and PowerPICC SOLO catheters
- FDA Device
- Class II
- terminated
- Published 2015-09-30
On 2015-09-30 the FDA classified a Class II recall of Marketing brochures for the PowerPICC and PowerPICC SOLO catheters by Bard Access Systems, citing bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to incorrect indication for use contained in the brochure.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2808-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-20 |
| Published | 2015-09-30 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Bard Access Systems |
| Distribution | n/a |
Product
Marketing brochures for the PowerPICC and PowerPICC SOLO catheters
Reason
Bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to incorrect indication for use contained in the brochure.
Identifiers
| code_info | The brochures were purchased from the vendor on 04/14/2015, Code S120667R0 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2808-2015%22
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