FDA Device recall Z-0943-2015
Nerve Block Tray (Nerve Block convenience kit)
- FDA Device
- Class II
- terminated
- Published 2015-01-14
On 2015-01-14 the FDA classified a Class II recall of Nerve Block Tray (Nerve Block convenience kit) by Centurion Medical Products, citing according to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hospira identified the particula….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0943-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-10-23 |
| Published | 2015-01-14 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Centurion Medical Products |
| Distribution | US |
Product
Nerve Block Tray (Nerve Block convenience kit)
Reason
According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hospira identified the particulate as human hair, embedded in and attached to a pinched area of the stopper.
Identifiers
| code_info | CMP Kit code: DT13405 Lot numbers: 2014061250 and 2014071750 Expiration date lot 2014061250: 2016-02 Expiration date lot 2014071750: 2016-03 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0943-2015%22
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