Home / Recalls / Stryker Sustainability Solutions / Z-2096-2016

Z-2096-2016 Class I Terminated

Recalled by Stryker Sustainability Solutions — Tempe, AZ

FDA device recall Z-2096-2016 was initiated by Stryker Sustainability Solutions on Jun 1, 2016 and is designated Class I. Reason for recall: Product defect; tip of two (2) Angiographic Catheters model # 10732203 broke off, prior to being used on the patient. The recall status is terminated (terminated Oct 19, 2016). Affected quantity: 167.

Recall Details

Product Type: Devices
Report Date: Jul 27, 2016
Initiation Date: Jun 1, 2016
Termination Date: Oct 19, 2016
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 167

Product Description

AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203

Reason for Recall

Product defect; tip of two (2) Angiographic Catheters model # 10732203 broke off, prior to being used on the patient.

Distribution Pattern

Worldwide Distribution -- USA, to the states of TX, UT, PA, CA, VT, MA, WA, VA, NY, MD, and CT; and, the country of CANADA.

Code Information

Item Lot Manufacturing Number Number Date Expiration Date 10732203 119965U 11/7/2003 N/A 10732203 158623U 12/2/2003 N/A 10732203 175183U 3/22/2005 N/A 10732203 179688U 10/29/2004 N/A 10732203 191185U 12/5/2004 N/A 10732203 210813U 7/1/2005 N/A 10732203 225911U 10/27/2005 N/A 10732203 225918U 10/19/2005 N/A 10732203 225919U 10/17/2005 N/A 10732203 8248U 1/31/2006 N/A 10732203 253202U 2/23/2006 N/A 10732203 277726U 7/21/2006 N/A 10732203 302844U 12/14/2006 N/A 10732203 309329U 11/16/2006 N/A 10732203 325680U 12/30/2006 N/A 10732203 343908U 8/2/2008 N/A 10732203 352756U 8/11/2008 N/A 10732203 352761U 9/3/2008 N/A 10732203 359352U 2/6/2008 N/A 10732203 363987U 5/17/2008 N/A 10732203 366572U 10/18/2008 N/A 10732203 369818U 9/27/2008 N/A 10732203 375883U 9/20/2008 N/A 10732203 772102U 8/5/2004 N/A 10732203 773196U 12/18/2004 N/A 10732203 773216U 1/6/2005 N/A 10732203 775985U 3/16/2005 N/A 10732203 7710750U 8/3/2006 N/A

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-2096-2016
openFDA file date: Oct 23, 2026
Loaded by RegDataLab: Oct 25, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.