PowerPort Slim Implantable Port — Class II medical device recall Z-1300-2014
Terminated recall by Bard Access Systems, reported 2014-04-02, distributed nationwide. Labeling discrepancy.The label states that the implantable port contains silicone suture plugs, however approx
| Recall number | Z-1300-2014 |
|---|---|
| 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 | 2014-02-27 |
| Classified | 2014-03-27 |
| Reported by FDA | 2014-04-02 |
| Terminated | 2014-09-05 |
| Distributed | Nationwide (US) |
| Quantity | 777 |
| Reason classes | labeling |
| Lot numbers | REXA1302, REXA1350, REXB1160 |
Product
PowerPort Slim Implantable Port, indicated for patient therapies requiring repeated access to the vascular system. Product Codes: 1716000, 1716070
Reason for recall
Labeling discrepancy.The label states that the implantable port contains silicone suture plugs, however approximately 23% of the units contained in the affected lots have a PowerPort Slim titanium implantable port without silicone suture plugs.
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-1300-2014. 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.