Home › Device types › GBW
Catheter, Peritoneal
FDA product code GBW · Class 1 · General, Plastic Surgery
98
Registered devices
124
Adverse events
15
Recalls
17
510(k) clearances
Devices with this code
Cook — COOK INCORPORATEDTenckhoff — COOK INCORPORATEDCook — COOK INCORPORATEDTAUT — TELEFLEX INCORPORATEDStylet — Medionics International IncCook — COOK INCORPORATEDMedline — MEDLINE INDUSTRIES, INC.CORE DYNAMICS — Conmed CorporationDeRoyal — DEROYAL INDUSTRIES, INC.TAUT — TELEFLEX INCORPORATEDARROW — TELEFLEX INCORPORATEDCook — COOK INCORPORATEDTenckhoff — COOK INCORPORATEDCook — COOK INCORPORATEDCARDINAL HEALTH — Cardinal Health 200, LLCSilicone Sump Drain Tube — FORTUNE MEDICAL INSTRUMENT CORP.Cook — COOK INCORPORATEDStenting Malecot — BOSTON SCIENTIFIC CORPORATIONTenckhoff — COOK INCORPORATEDCORE DYNAMICS — Conmed CorporationGrafco — GF HEALTH PRODUCTS, INC.TAUT — TELEFLEX INCORPORATEDTenckhoff — COOK INCORPORATEDTAUT — TELEFLEX INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-21 | ARROW INTERNATIONAL, LLC | Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality iss |
| 2017-12-12 | Boston Scientific Corporation | Certain Malecot Nephrostomy Catheters are breaking at the mid-shaft bond during use. |
| 2016-06-27 | ConMed Corporation | The packaging seal may contain a crease. The crease may result in an open channel. These channels may compromise sterility of the product. |
| 2016-06-27 | ConMed Corporation | The packaging seal may contain a crease. The crease may result in an open channel. These channels may compromise sterility of the product. |
| 2016-06-27 | ConMed Corporation | The packaging seal may contain a crease. The crease may result in an open channel. These channels may compromise sterility of the product. |
| 2016-06-27 | ConMed Corporation | The packaging seal may contain a crease. The crease may result in an open channel. These channels may compromise sterility of the product. |
| 2016-06-27 | ConMed Corporation | The packaging seal may contain a crease. The crease may result in an open channel. These channels may compromise sterility of the product. |
| 2016-06-27 | ConMed Corporation | The packaging seal may contain a crease. The crease may result in an open channel. These channels may compromise sterility of the product. |
| 2015-10-14 | Teleflex Medical | The defective component can cause gas leakage through the device. This can result in loss of pneumoperitoneum, potentially necessitating removal of the defect |
| 2012-07-20 | Teleflex Medical | Product is missing the label on the internal packaging. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.