POWERWAND Safety Introducer with Extended Dwell Catheter — Class II medical device recall Z-2254-2013
Terminated recall by Access Scientific Inc, reported 2013-09-25, distributed in MI, TX. Access Scientific is recalling the POWERWAND Saftey Introducer with Extended Dwell Catheter because it is misl
| Recall number | Z-2254-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Access Scientific Inc, San Diego, CA, United States |
| Recall initiated | 2013-08-16 |
| Classified | 2013-09-18 |
| Reported by FDA | 2013-09-25 |
| Terminated | 2013-09-24 |
| Distributed | MI, TX |
| Quantity | 160 units |
| Reason classes | labeling |
| Lot numbers | I666473 |
| Model numbers | 92006 |
Product
POWERWAND Safety Introducer with Extended Dwell Catheter; Catalog no. 92006. Used to gain access to the vascular system to sample blood and administer fluids intravenously.
Reason for recall
Access Scientific is recalling the POWERWAND Saftey Introducer with Extended Dwell Catheter because it is mislabeled.
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-2254-2013. 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.