FDA Device recall Z-1233-2017
Jackson-Pratt Channel Drain Silicone Round, Fully Fluted w/10FR Trocar
- FDA Device
- Class II
- terminated
- Published 2017-03-01
On 2017-03-01 the FDA classified a Class II recall of Jackson-Pratt Channel Drain Silicone Round, Fully Fluted w/10FR Trocar by Degania Silicone, citing product sterility compromised due to breach of sterile barrier.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1233-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-01-31 |
| Published | 2017-03-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Degania Silicone |
| Distribution | PR |
Product
Jackson-Pratt Channel Drain Silicone Round, Fully Fluted w/10FR Trocar. Sterile. Rx Distributed by Cardinal Health, USA Catalog Number: JP-2187 For wound drainage.
Reason
Product sterility compromised due to breach of sterile barrier
Identifiers
| code_info | Lot Number: P1546816 Expiration date: January 2021 |
|---|
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-1233-2017%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.