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COOK INCORPORATED · Model G19089 · UDI-DI 00827002190894
KOB
Prescription
10
510(k) clearances
205
Adverse events (1 deaths)
66
Recalls
23
Facilities
Description
Neonatal Percutaneous Pigtail Nephrostomy Set
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-04-22 | Cook Inc. | Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative Pyeloplasty Stent Set Instructions for Use (IFU) did not include a warning for stent knotting. |
| 2019-04-22 | Cook Inc. | Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative Pyeloplasty Stent Set Instructions for Use (IFU) did not include a warning for stent knotting. |
| 2019-01-04 | Cook Inc. | The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip. |
| 2019-01-04 | Cook Inc. | The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip. |
| 2005-07-22 | Boston Scientific Corporation | The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use. |
| 2005-07-22 | Boston Scientific Corporation | The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use. |
| 2005-07-22 | Boston Scientific Corporation | The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use. |
| 2005-07-22 | Boston Scientific Corporation | The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use. |
| 2005-07-22 | Boston Scientific Corporation | The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use. |
| 2005-07-22 | Boston Scientific Corporation | The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
