FDA Device recall Z-0781-2018
AVID TruCustom DJ'S VASCULAR/NEURO TRAY convenience kits, Item Code: AV010930-12
- FDA Device
- Class II
- terminated
- Published 2018-03-07
On 2018-03-07 the FDA classified a Class II recall of AVID TruCustom DJ'S VASCULAR/NEURO TRAY convenience kits, Item Code: AV010930-12 by Avid Medical, citing certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specificati….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0781-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-22 |
| Published | 2018-03-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Avid Medical |
| Distribution | IL, KY, LA, MA, MO, NY, OH, TX, VA, WI |
Product
AVID TruCustom DJ'S VASCULAR/NEURO TRAY convenience kits, Item Code: AV010930-12
Reason
Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
Identifiers
| code_info | Lot, Expiration Date: 1205011 8/1/2019 1213805 10/1/2019 |
|---|
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-0781-2018%22
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