Arrow International — Class II medical device recall Z-1823-2012
Terminated recall by Arrow International Inc, reported 2012-06-27, distributed nationwide. Arrow is recalling the product due to the possibility of voids in the catheter hub which could lead to an inte
| Recall number | Z-1823-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2012-06-07 |
| Classified | 2012-06-19 |
| Reported by FDA | 2012-06-27 |
| Terminated | 2014-04-03 |
| Distributed | Nationwide (US) |
| Quantity | 1,085 |
| Lot numbers | RF2033361 |
| Model numbers | CDC-42703-XP1A |
Product
Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog number CDC-42703-XP1A The multiple-lumen pressure injectable catheter permits venous access to central circulation and injection of contrast media. The ARROWg+ard(R) antimicrobial surface is intended to provide protection against catheter-related infections.
Reason for recall
Arrow is recalling the product due to the possibility of voids in the catheter hub which could lead to an interlumen crossover.
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-1823-2012. 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.