FDA Device recall Z-1426-2018
Thoracentesis/ Paracentesis Kit 10/CS
- FDA Device
- Class II
- terminated
- Published 2018-04-25
On 2018-04-25 the FDA classified a Class II recall of Thoracentesis/ Paracentesis Kit 10/CS by Carefusion 2200, citing the integrity of the sterile packaging is potentially compromised.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1426-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-23 |
| Published | 2018-04-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Carefusion 2200 |
| Distribution | US |
Product
Thoracentesis/ Paracentesis Kit 10/CS; STERILE;
Reason
The integrity of the sterile packaging is potentially compromised.
Identifiers
| code_info | Product Code: TPK1001 / LOT 0000837811, 0000842215, 0000840336, 0000851185 |
|---|
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-1426-2018%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.