Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0031-2015 — PICC Convenience Kit with Accessories, BioFlo PICC with ENDEXO and PASV Valve Technology, 5F-55 cm SINGLE LUMEN, UPN Product No. H96560M1406071, REF/Catalog No. 60M140607, STERILE --- Navilyst Medical, Inc. 10 Glens Falls Technical Park Glens Falls, NY 12801

U.S. FDA — Device Enforcement · United States · 2014-08-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0031-2015
Date of alert
2014-08-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Navilyst Medical, Inc
Product category
device
Product type
Devices
Reported risk: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline Flush Syringes, that it had initiated a recall on specific lots of the syringes as some syringe unit packages exhibited open seals which may impact package integrity and potentially affect product sterility. Based on the notification, NMI is recalling specific PICC Kits that contain the affected 10 ml BD PosiFlush SF Saline Flush Syringes.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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