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Vygon Corp.

Last updated May 23, 2026

Information

Country: US
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Catalogue (1773)

Page 8 of 36

Device	Model / Reference	Registries	Class	Status
Vygon	625.08	FDA UDI	Class I	Active
Vygon	AMS-8423CP	FDA UDI	Class II	Active
Vygon	AMS-7090	FDA UDI	Class II	Active
Vygon	CMS-809-2	FDA UDI	Class II	Active
Vygon	542.10	FDA UDI	Class I	Active
Vygon	310.07	FDA UDI	Class II	Unknown
Vygon	340.12	FDA UDI	Class II	Unknown
Vygon	311.10	FDA UDI	Class II	Unknown
Vygon	828.01	FDA UDI	Class II	Active
Vygon	AMS-9579CP-3	FDA UDI	Class I	Active
Vygon	542.14	FDA UDI	Class I	Active
Vygon	BN-762	FDA UDI	Class II	Active
Vygon	VYML5D1001	FDA UDI	Class II	Active
Vygon	VAMST6.0	FDA UDI	Class II	Active
Vygon	AMS-9817CP-3	FDA UDI	Class I	Active
Vygon	AMS-437	FDA UDI	Class II	Active
Vygon	820.22	FDA UDI	Class I	Active
Vygon	312.10	FDA UDI	Class II	Active
Vygon	363.122	FDA UDI	Class II	Active
Vygon	SHY-1910	FDA UDI	Class II	Active
Vygon	SS-395B	FDA UDI	Class II	Active
Vygon	AMS-8181CP	FDA UDI	Class II	Active
Vygon	CMS-862	FDA UDI	Class II	Active
Vygon	AMS-9788CP-3A	FDA UDI	Class I	Active
Vygon	220.020	FDA UDI	Class II	Active
Vygon	310.08	FDA UDI	Class II	Active
Vygon	AMS-9837CP-7A	FDA UDI	Class II	Active
Vygon	AMS-7200	FDA UDI	Class I	Active
Vygon	821.21	FDA UDI	Class II	Active
Vygon	AMS-729CP-3	FDA UDI	Class I	Active
Vygon	AMS-400	FDA UDI	Class II	Active
Vygon	AMS-9860-1	FDA UDI	Class I	Active
Vygon	311.08	FDA UDI	Class II	Unknown
Vygon	5562.413	FDA UDI	Class II	Active
Vygon	VYML5D3001SK	FDA UDI	Class II	Active
Nutriline Twinflo	1252.232G	FDA UDI	Class II	Active
Vygon	1363.102	FDA UDI	Class II	Unknown
Vygon	AMS-923CP	FDA UDI	Class II	Active
Vygon	VY-MAX	FDA UDI	Class II	Active
Vygon	AMS-8952CP-2	FDA UDI	Class I	Active
Vygon	AMS-483C	FDA UDI	Class II	Active
Vygon	VYLF5008	FDA UDI	Class II	Active
Vygon	CLG-2050	FDA UDI	Class II	Active
Vygon	1270.04	FDA UDI	Class II	Active
Vygon	AMS-290	FDA UDI	Class II	Active
Vygon	311.10	FDA UDI	Class II	Active
Vygon	361.067	FDA UDI	Class II	Active
Vygon	361.062	FDA UDI	Class II	Active
Vygon	542.06	FDA UDI	Class I	Active
Vygon	1311.05	FDA UDI	Class II	Unknown

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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.