Pericardiocentesis Set — Class II medical device recall Z-1565-2020
Terminated recall by Cook Inc., reported 2020-04-01, distributed in CO, DE, MD, MN, NC, NV, WV. The printed expiration dates are incorrect.
| Recall number | Z-1565-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cook Inc., Bloomington, IN, United States |
| Recall initiated | 2020-03-06 |
| Classified | 2020-03-24 |
| Reported by FDA | 2020-04-01 |
| Terminated | 2020-12-18 |
| Distributed | CO, DE, MD, MN, NC, NV, WV |
| Countries outside the US | CA |
| Quantity | 25 |
| UPC / GTIN / UDI-DI | 00827002106437 |
| Lot numbers | 10119247 |
| Model numbers | C-PCS-700-TORONT0-042997 |
Product
Pericardiocentesis Set, Irrigation Catheter, Reference Part Number C-PCS-700-TORONT0-042997, Order Number G10643
Reason for recall
The printed expiration dates are incorrect.
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-1565-2020. 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.