Vascular Solutions, Inc.: 10 recalls on record

Recalls filed with 1 agency: FDA (10).

First recall on record: September 26, 2012. Most recent: June 27, 2018.

Risk classification: Class I: 5 · Class II: 5

Most recent recalls

DateAgencyProduct
June 27, 2018FDADrainer(R) Centesis Catheters: (a) REF 8810, 5F x 9cm (b) REF 8811, 6F x 9cm (c) REF 8…Z-2249-2018
June 7, 2017FDADolphin Inflation Device, REF 0185NA. Rx only, Sterilized using Ethylene Oxide. DOL…Z-2180-2017
March 1, 2017FDAGrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usa…Z-1250-2017
October 26, 2016FDAVascular Solutions Twin-Pass .023" Dual Access Catheter, model 5230. Sterilized with Eth…Z-0055-2017
October 26, 2016FDAVascular Solutions Twin-Pass RX Dual Access Catheter, model 5210. Sterilized with Ethyle…Z-0054-2017
April 13, 2016FDAGuardian II Hemostasis Valve, models 8210 and 8211. The following models are only availa…Z-1275-2016
July 9, 2014FDALangston Dual Lumen Catheters, 6Fr, REF 5550 and 5540. The Vascular Solutions Langston Du…Z-1981-2014
March 27, 2013FDAVascular Solutions, Inc., Guardian II and Guardian II NC Hemostasis Valve, used in cardio…Z-0955-2013
February 27, 2013FDAVascular Solutions, SuperCross Microcatheter, Sterilized using ethylene oxide, Rx Only, M…Z-0868-2013
September 26, 2012FDAGuardian II Hemostasis Valve, Model 8210 and Guardian II NC Hemostasis Valve, Model FH102…Z-2400-2012

Questions about this company

How many recalls does Vascular Solutions, Inc. have?
Recalert has 10 U.S. recalls on record for Vascular Solutions, Inc., published between September 26, 2012 and June 27, 2018.
What was the most recent Vascular Solutions, Inc. recall?
FDA recall Z-2249-2018, published June 27, 2018: Drainer(R) Centesis Catheters: (a) REF 8810, 5F x 9cm (b) REF 8811, 6F x 9cm (c) REF 8812, 5F x 15cm Product The Drainer centesis catheter is intended for use in percutaneous fluid aspirations …
Which agencies have handled Vascular Solutions, Inc. recalls?
Vascular Solutions, Inc. appears as the recalling firm in recalls from: FDA (10).

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