Jackson-Pratt Channel Drain Silicone Round — Class II medical device recall Z-1233-2017
Terminated recall by Degania Silicone, Ltd., reported 2017-03-01, distributed in PR. Product sterility compromised due to breach of sterile barrier
| Recall number | Z-1233-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Degania Silicone, Ltd., Dganya Bet, N/A, Israel |
| Recall initiated | 2017-01-31 |
| Classified | 2017-02-22 |
| Reported by FDA | 2017-03-01 |
| Terminated | 2017-04-04 |
| Distributed | PR |
| Quantity | 3,040 units |
| Reason classes | sterility |
| Lot numbers | P1546816 |
| Model numbers | JP-2187 |
| Expiration dates | 2021-01-20 |
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 for recall
Product sterility compromised due to breach of sterile barrier
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1233-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.