PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer — Class III medical device recall Z-2050-2015
Terminated recall by Bard Access Systems, reported 2015-07-15, distributed nationwide. Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to incorrect expiration dates on the primary
| Recall number | Z-2050-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bard Access Systems, Salt Lake City, UT, United States |
| Recall initiated | 2015-05-27 |
| Classified | 2015-07-08 |
| Reported by FDA | 2015-07-15 |
| Terminated | 2016-02-10 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| Lot numbers | REYK1761 |
| Model numbers | 9194108D |
Product
PowerPICC SOLO2 Catheter 4F Maximal Barrier Tray with Microintroducer (Single-Lumen) (Sherlock) The PowerPICC Solo catheters are intended for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling.
Reason for recall
Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to incorrect expiration dates on the primary labeling.
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-2050-2015. 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.