FDA Device recall Z-0942-2015
Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)
- FDA Device
- Class II
- terminated
- Published 2015-01-14
On 2015-01-14 the FDA classified a Class II recall of Chest Tube Tray (Cardiovascular Surgical Instruments 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-0942-2015 |
| 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
Chest Tube Tray (Cardiovascular Surgical Instruments 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: CHT900 Lot numbers: 2014061950 and 2014070750 Expiration date, both lots: 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-0942-2015%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.