Home › Device types › PTI
Non-Coring (Huber) Needle
FDA product code PTI · Class 2 · General Hospital
126
Registered devices
154
Adverse events
12
Recalls
13
510(k) clearances
Devices with this code
MEDLINE — MEDLINE INDUSTRIES, INC.Infusion Safety Products, Inc. — INFUSION SAFETY PRODUCTS, INC.Port Access — Bard Access Systems, Inc.SafeStep — Bard Access Systems, Inc.MEDLINE — MEDLINE INDUSTRIES, INC.SURECAN SAFETY II — B. BRAUN MEDICAL INC.Infusion Safety Products, Inc. — INFUSION SAFETY PRODUCTS, INC.Infusion Safety Products, Inc. — INFUSION SAFETY PRODUCTS, INC.AllPoints Port Access System PowerLoc Max — Bard Access Systems, Inc.SURECAN SAFETY II — B. BRAUN MEDICAL INC.Infusion Safety Products, Inc. — INFUSION SAFETY PRODUCTS, INC.Infusion Safety Products, Inc. — INFUSION SAFETY PRODUCTS, INC.MEDLINE — MEDLINE INDUSTRIES, INC.Infusion Safety Products, Inc. — INFUSION SAFETY PRODUCTS, INC.SURECAN SAFETY II — B. BRAUN MEDICAL INC.Port Access — Bard Access Systems, Inc.AllPoints Port Access System SafeStep — Bard Access Systems, Inc.AllPoints Port Access System PowerLoc Max — Bard Access Systems, Inc.MEDLINE — MEDLINE INDUSTRIES, INC.Port Access — Bard Access Systems, Inc.MEDLINE — MEDLINE INDUSTRIES, INC.SURECAN SAFETY II — B. BRAUN MEDICAL INC.INTERA — Intera Oncology Inc.Port Access — Bard Access Systems, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-06-19 | Becton Dickinson & Company | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage re |
| 2020-06-19 | Becton Dickinson & Company | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage re |
| 2020-06-19 | Becton Dickinson & Company | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage re |
| 2020-06-19 | Becton Dickinson & Company | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage re |
| 2020-06-19 | Becton Dickinson & Company | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage re |
| 2020-06-19 | Becton Dickinson & Company | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage re |
| 2020-06-19 | Becton Dickinson & Company | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage re |
| 2020-06-19 | Becton Dickinson & Company | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage re |
| 2020-06-19 | Becton Dickinson & Company | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage re |
| 2020-06-19 | Becton Dickinson & Company | Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage re |
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.
