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Sign in to claim this brandVygon Corp.
US
Last updated May 23, 2026
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Catalogue (1773)
Page 5 of 36| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vygon | AMS-884-2T | FDA UDI | Class II | Active |
| Vygon | AMS-588 | FDA UDI | Class II | Active |
| Vygon | 363.102 | FDA UDI | Class II | Active |
| Vygon | VAMST4.0 | FDA UDI | Class II | Active |
| Vygon | MBS-2010 | FDA UDI | Class II | Active |
| Vygon | 5805.01 | FDA UDI | Class I | Active |
| Vygon | CLGY-1934 | FDA UDI | Class II | Active |
| Vygon | BN-448 | FDA UDI | Class II | Active |
| Vygon | AMS-744CP | FDA UDI | Class II | Active |
| Vygon | AMS-7104CP | FDA UDI | Class I | Active |
| Vygon | AMS-9501-3 | FDA UDI | Class II | Active |
| Vygon | 1362.187 | FDA UDI | Class II | Active |
| Vygon | 1362.107 | FDA UDI | Class II | Active |
| Vygon | AMS-7517CPA | FDA UDI | Class II | Active |
| Vygon | AMS-845CS-1 | FDA UDI | Class II | Active |
| Vygon | AMS-477 | FDA UDI | Class II | Active |
| Vygon | 1363.1621 | FDA UDI | Class II | Active |
| Churchill Medical Systems | BHY-2250 | FDA UDI | Class II | Active |
| Vygon | AMS-435CV-1 | FDA UDI | Class II | Active |
| Vygon | AMS-948 | FDA UDI | Class II | Active |
| Vygon | AMS-872CP-1 | FDA UDI | Class II | Active |
| Vygon | 1011.052 | FDA UDI | Class II | Active |
| Vygon | 1159.65 | FDA UDI | Class II | Active |
| Vygon | AMS-375-1 | FDA UDI | Class II | Active |
| Vygon | AMS-588 | FDA UDI | Class II | Active |
| Vygon | AMS-859CS-3 | FDA UDI | Class II | Active |
| Vygon | VYCIS012 | FDA UDI | Class II | Active |
| Vygon | 1361.082 | FDA UDI | Class II | Active |
| Vygon | 1340.08 | FDA UDI | Class II | Unknown |
| Vygon | 516.20 | FDA UDI | Class II | Active |
| Vygon | 366.187 | FDA UDI | Class II | Active |
| Vygon | BN-150 | FDA UDI | Class II | Active |
| Vygon | 366.167 | FDA UDI | Class II | Active |
| Vygon | AMS-9983CP-1A | FDA UDI | Class II | Active |
| Vygon | BN-300NS | FDA UDI | Class II | Active |
| Vygon | 1363.1421 | FDA UDI | Class II | Active |
| Vygon | AMS-8345CP-1 | FDA UDI | Class I | Active |
| Vygon | AMS-8346 | FDA UDI | Class I | Active |
| Vygon | 362.167 | FDA UDI | Class II | Active |
| Vygon | AMS-744CP | FDA UDI | Class II | Active |
| Vygon | VYPL5T3003A | FDA UDI | Class II | Active |
| Vygon | AMS-8023CP-1 | FDA UDI | Class II | Active |
| Vygon | CLG-2010-1 | FDA UDI | Class II | Active |
| Vygon | VYG45MN-R | FDA UDI | Class II | Active |
| Vygon | AMS-8952CP-4 | FDA UDI | Class I | Active |
| Vygon | 220.050 | FDA UDI | Class II | Active |
| Vygon | 1363.0821 | FDA UDI | Class II | Active |
| Vygon | 362.087 | FDA UDI | Class II | Active |
| Vygon | AMS-9837CP-7 | FDA UDI | Class II | Active |
| Vygon | 1311.08 | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (23)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Aug 28, 2014 | Z-0113-2015 | — | terminated | Vygon has uncovered potential problems with membrane elasticity in the 896.038, Bionector Needleless connector and is issuing a voluntary recall of the 896.038, Bionector Needleless connector. |
| Dec 17, 2012 | Z-0937-2013 | — | terminated | Product was packaged with the incorrect introducer needle. The kit label indicates a "safety" needle is included; the kits were packaged with a non-safety needle. |
| May 11, 2012 | Z-1798-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1806-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1801-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1808-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1807-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1800-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1805-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1797-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1804-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1803-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1799-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| May 11, 2012 | Z-1802-2012 | — | terminated | Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes. |
| Apr 26, 2011 | Z-2700-2011 | — | terminated | Peripherally inserted central catheter has the potential to leak or break at the hub while in use, which could lead to a loss of blood or catheter migration. |
| Apr 26, 2011 | Z-2699-2011 | — | terminated | Peripherally inserted central catheter has the potential to leak or break at the hub while in use, which could lead to a loss of blood or catheter migration. |
| Apr 19, 2011 | Z-2391-2011 | — | terminated | Skin-Prep wipes purchased by Churchill (a Vygon company) for inclusion into Dressing Kits and PICC Insertion Kits were recalled by the manufacturer due to potential bacterial contamination. |
| Apr 19, 2011 | Z-2389-2011 | — | terminated | Skin-Prep wipes purchased by Churchill (a Vygon company) for inclusion into Dressing Kits and PICC Insertion Kits were recalled by the manufacturer due to potential bacterial contamination. |
| Apr 19, 2011 | Z-2390-2011 | — | terminated | Skin-Prep wipes purchased by Churchill (a Vygon company) for inclusion into Dressing Kits and PICC Insertion Kits were recalled by the manufacturer due to potential bacterial contamination. |
| Apr 19, 2011 | Z-2388-2011 | — | terminated | Skin-Prep wipes purchased by Churchill (a Vygon company) for inclusion into Dressing Kits and PICC Insertion Kits were recalled by the manufacturer due to potential bacterial contamination. |
| Jun 27, 2005 | Z-0090-06 | — | terminated | Guidewire protuding from tip of the catheter |
| Apr 9, 2003 | Z-0849-03 | — | terminated | Nutriline with Peelable Sheath 2 Fr. and Neonatal Catheter & Insertion Tray were packaged with a 3 Fr. insertion sheath. |
| Apr 9, 2003 | Z-0850-03 | — | terminated | Nutriline with Peelable Sheath 2 Fr. and Neonatal Catheter & Insertion Tray were packaged with a 3 Fr. insertion sheath. |