# FDA recall Z-0282-2019 > **Arrow International Inc** · Class II · device recall initiated 2018-08-30. ## Product Arrow AGB + Multi-Lumen CVC Kit, Cat. No. CDC-42703-B1A. Product Usage - The Arrow CVC is intended to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access, including, but not limited to the following: Lack of usable peripheral IV sites, Central venous pressure monitoring, Total parenteral nutrition (TPN), Infusions of fluids, medications, or chemotherapy, and Frequent blood sampling or receiving blood transfusions/blood products. ## Reason for recall The product was shipped after its expiry date due to a system error. The product lidstock identifies the correct expiration date however the accompanying purchase order shipping documentation identifies an incorrect expiration date. Per standard clinical practice the lidstock would most likely be checked prior to use and the product would not be used leading to a minor delay while a replacement is located. In the unlikely event that the product lidstock is not checked prior to use, there is potential for use of expired product, and product functionality/or sterility cannot be guaranteed. ## Distribution US nationwide in the states of CA, FL, NC, and RI. ## Key facts - **Recall number:** Z-0282-2019 - **Recalling firm:** Arrow International Inc - **Classification:** Class II - **Product type:** device - **Status:** Terminated - **Initiation date:** 2018-08-30 - **Report date:** 2018-11-07 - **Termination date:** 2020-07-31 - **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-0282-2019 ## Citation > AI Analytics. FDA recall Z-0282-2019. Retrieved 2026-07-12 from https://api.ai-analytics.org/recall/Z-0282-2019. Source: US FDA. Licensed CC0. --- *[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*