# FDA recall Z-2398-2020 > **Angiodynamics, Inc.** · Class II · device recall initiated 2020-05-04. ## Product BioFlo PICC and Xcela PICC Maximal Barrier Nursing Kits - Product Usage: are indicated for short or long-term peripheral access to the central venous system for intravenous therapy, including but not limited to, the administration of fluids, medications and nutrients; the sampling of blood; and for power injection of contrast media. Item Numbers H965750011 H965750031 H965750121 H965750131 H965750141 H965750151 H965750161 H965750171 H965750181 H965750191 H965750211 H965750221 H965750231 H965750241 H965750315 H965750315-NP H965750325 H965750335 H965750335-NP H965750345 H965750355 H965750355-NP H965750365 H965750375 H965750385 H965750415 H965750425 H965750441 H965750451 H965750471 H965750481 H965750491 H965750501 H965750521 H965750531 H965750541 H965750551 H965750561 H965750571 H965750581 H965750591 H965750601 H965750611 H965750621 H965750631 H965750651 H965750661 H965750671 H965750681 H965750691 H965750701 Cat. No. 75-001 75-003 ## Reason for recall Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020. ## Distribution US Nationwide distribution. ## Key facts - **Recall number:** Z-2398-2020 - **Recalling firm:** Angiodynamics, Inc. - **Classification:** Class II - **Product type:** device - **Status:** Terminated - **Initiation date:** 2020-05-04 - **Report date:** 2020-06-24 - **Termination date:** 2023-08-23 - **Voluntary/Mandated:** Voluntary: Firm initiated - **Location:** Queensbury, NY, United States ## Primary source FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2398-2020 ## Citation > AI Analytics. FDA recall Z-2398-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2398-2020. Source: US FDA. Licensed CC0. --- *[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*