FDA Device recall Z-2096-2016
AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203
- FDA Device
- Class I
- terminated
- Published 2016-07-27
On 2016-07-27 the FDA classified a Class I recall of AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203 by Stryker Sustainability Solutions, citing product defect; tip of two (2) Angiographic Catheters model # 10732203 broke off, prior to being used on the patient.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2096-2016 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2016-06-01 |
| Published | 2016-07-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Sustainability Solutions |
| Distribution | CA, CT, MA, MD, NY, PA, TX, UT, VA, VT, WA |
Product
AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203
Reason
Product defect; tip of two (2) Angiographic Catheters model # 10732203 broke off, prior to being used on the patient.
Identifiers
| code_info | Item Lot Manufacturing Number Number Date Expiration Date 10732203 119965U 11/7/2003…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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2096-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.