Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip — Class I medical device recall Z-1830-2012
Terminated recall by Arrow International Inc, reported 2012-07-04, distributed nationwide. Lidstock of product does not contain chlorhexidine contraindication and contains wording "contains no medicati
| Recall number | Z-1830-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2012-05-03 |
| Classified | 2012-06-26 |
| Reported by FDA | 2012-07-04 |
| Terminated | 2013-03-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, BH, CA, CH, CL, CO, CR, CY, CZ, DE, DK, DO, EE, ES, FI, FR, GB, GR, GT, HU, IE, IN, IT, KE, KW, LB, LT, LU, LV, NL, NO, NZ, OM, PL, PT, QA, RO, RS, SA, SG, SI, SK, TR, UA, ZA |
| Quantity | 634,912 |
| Reason classes | labeling |
| Lot numbers | 22802, 25123-F, AD-24703-OB, AD-24730-E, AD-24730-OB, AD-24730-OL, AD-24802, AD-24854, AD-24854-NL, AD-25703, AD-25802-OB, AD-25855, AD-26702, AG-25854-E, ARCS-22122-F, ARCS-22123-F, ARCS-22703-E, ARCS-22802, ARCS-22854-E, ARCS-22855, ARCS-25854-E, ARCS-25855, ARCS-25855-E, ARCS-26553, ARCV-20854, ARCV-22703, ARCV-22854, ARCV-25854, AT-25854-E, AT-25855, AT-25855-E, B-22853, BB-09903-AG, BB-22122-F, BB-22123-F, BCV-27702-EJT, BERGAMO-25703-E, BERGAMO-27702-E, BK-22703, BL-22702 and 460 more |
| Model numbers | 22802, 25123-F, AD-24703, AD-24703-OB, AD-24730-E, AD-24730-OB, AD-24730-OL, AD-24802, AD-24854, AD-24854-NL, AD-25703, AD-25802-OB, AD-25855, AD-26702, AG-25854-E, ARCS-22122-F, ARCS-22123-F, ARCS-22703-E, ARCS-22802, ARCS-22854-E, ARCS-22855, ARCS-25854-E, ARCS-25855, ARCS-25855-E, ARCS-26553 and 475 more |
Product
Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) ARROWgard Blue(R) Catheter Product Usage: The multiple-lumen catheter permits venous access to central circulation.
Reason for recall
Lidstock of product does not contain chlorhexidine contraindication and contains wording "contains no medication" on the label. Product insert does reflect medicated status.
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-1830-2012. 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.