Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for venous… — Class II medical device recall Z-1106-2021
Terminated recall by Arrow International Inc, reported 2021-02-17, distributed nationwide. The lidstock / information card on the kits correctly states the product code as CDC-45703-1A. The banner card
| Recall number | Z-1106-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2021-01-06 |
| Classified | 2021-02-10 |
| Reported by FDA | 2021-02-17 |
| Terminated | 2022-07-12 |
| Distributed | Nationwide (US) |
| Quantity | 1,705 eaches |
| Lot numbers | 13F20E0173 |
Product
Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for venous access to the central circulation by the way of the femoral, jugular, or subclavian veins. Product Code: CDC-45703-1A
Reason for recall
The lidstock / information card on the kits correctly states the product code as CDC-45703-1A. The banner card on the side of the kit may incorrectly state the product code as CDC-15703-1A and not identify the product as a coated ARROWg+ard Blue PLUS (AGB+) antimicrobial catheter which may cause a minor delay during use and placement of a coated catheter in patients with known sensitivity to chlorohexidine, silver sulfadiazine or sulfa could result in an allergic reaction
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-1106-2021. 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.