FDA Device recall Z-1722-2019
Pericardiocentesis Catheter Set, RPN C-PCS-850, Order # G03282
- FDA Device
- Class II
- terminated
- Published 2019-06-12
On 2019-06-12 the FDA classified a Class II recall of Pericardiocentesis Catheter Set, RPN C-PCS-850, Order # G03282 by Cook, citing affected products may have been manufactured with the catheter distal end hole too small.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1722-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-04-09 |
| Published | 2019-06-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Cook |
| Distribution | OH |
Product
Pericardiocentesis Catheter Set, RPN C-PCS-850, Order # G03282
Reason
Affected products may have been manufactured with the catheter distal end hole too small
Identifiers
| code_info | Lot Numbers 7716007 7703324 NS7703501 NS7703502 NS7703503 NS7704718 NS7704722 NS7704727 NS7704728 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1722-2019%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.