# FDA recall Z-1106-2021

> **Arrow International Inc** · Class II · device recall initiated 2021-01-06.

## 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

## Distribution

US Nationwide

## Key facts

- **Recall number:** Z-1106-2021
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-01-06
- **Report date:** 2021-02-17
- **Termination date:** 2022-07-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Reading, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1106-2021

## Citation

> AI Analytics. FDA recall Z-1106-2021. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-1106-2021. Source: US FDA. Licensed CC0.

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