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Vygon Corp.

Last updated May 23, 2026

Information

Country: US
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Catalogue (1773)

Page 7 of 36

Device	Model / Reference	Registries	Class	Status
Vygon	AMS-836	FDA UDI	Class II	Active
Vygon	180.05	FDA UDI	Class II	Active
Vygon	VYPL6T1001	FDA UDI	Class II	Active
Vygon	BN-3082CV	FDA UDI	Class II	Active
Vygon	AMS-7296CP	FDA UDI	Class I	Active
Vygon	1363.047	FDA UDI	Class II	Active
Vygon	CLG-2010	FDA UDI	Class II	Active
Vygon	5382.06	FDA UDI	Class II	Active
Vygon	SS-112-1	FDA UDI	Class II	Active
Vygon	AMS-9038CS	FDA UDI	Class II	Active
Vygon	AMS-7074CP-2A	FDA UDI	Class II	Active
Vygon	VYLF1006	FDA UDI	Class II	Active
Vygon	AMS-900CV	FDA UDI	Class II	Active
Vygon	KS-122-2	FDA UDI	Class II	Active
Vygon	AMS-483CNS	FDA UDI	Class II	Active
Vygon	362.182	FDA UDI	Class II	Active
Vygon	5562.513	FDA UDI	Class II	Active
Vygon	364.062	FDA UDI	Class II	Active
Vygon	CLGY-2034	FDA UDI	Class II	Active
Vygon	VYML4S0001	FDA UDI	Class II	Active
Vygon	AMS-8526CP-3	FDA UDI	Class II	Active
Vygon	BN-160	FDA UDI	Class II	Active
Vygon	5576.02	FDA UDI	Class I	Active
Premicath	1261.203G	FDA UDI	Class II	Active
Vygon	VYG70MN-R	FDA UDI	Class II	Active
Vygon	AMS-9849-1	FDA UDI	Class I	Active
Vygon	1366.1271	FDA UDI	Class II	Active
Vygon	AMS-8180-3CP	FDA UDI	Class II	Active
Vygon	AMS-9082	FDA UDI	Class II	Active
Vygon	AMS-872CP-1	FDA UDI	Class II	Active
Vygon	AMS-637B	FDA UDI	Class II	Active
Vygon	38.30.30	FDA UDI	Class II	Active
Vygon	391.06	FDA UDI	Class II	Unknown
Vygon	AMS-945	FDA UDI	Class II	Active
Vygon	AMS-537	FDA UDI	Class II	Active
Vygon	1340.16	FDA UDI	Class II	Active
Vygon	AMS-9734	FDA UDI	Class II	Active
Vygon	BN-3083CV	FDA UDI	Class II	Active
Vygon	AMS-802	FDA UDI	Class II	Active
Vygon	AMS-9958CP	FDA UDI	Class I	Active
Vygon	VYPL5T0001	FDA UDI	Class II	Active
Vygon	VAMST5.5	FDA UDI	Class II	Active
Vygon	AMS-782-2	FDA UDI	Class I	Active
Vygon	AMS-802-1	FDA UDI	Class II	Active
Vygon	AMS-819	FDA UDI	Class II	Active
Vygon	1366.1471	FDA UDI	Class II	Active
Vygon	81363.062F	FDA UDI	Class II	Active
Vygon	VYG130MN-R	FDA UDI	Class II	Active
Vygon	391.14	FDA UDI	Class II	Unknown
Vygon	MSY-2015	FDA UDI	Class II	Active

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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.