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Vygon Corp.

Last updated May 23, 2026

Information

Country: US
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Catalogue (1773)

Page 3 of 36

Device	Model / Reference	Registries	Class	Status
Vygon	AMS-7160CP	FDA UDI	Class II	Active
Vygon	AMS-938-3	FDA UDI	Class II	Active
Vygon	340.18	FDA UDI	Class II	Active
Vygon	1362.182	FDA UDI	Class II	Active
Vygon	AMS-8508CP-3	FDA UDI	Class II	Active
Vygon	AMS-823CP	FDA UDI	Class II	Active
Premicath	1261.203G	FDA UDI	Class II	Active
Vygon	AMS-975-1	FDA UDI	Class II	Active
Vygon	AMS-9147CP	FDA UDI	Class II	Active
Vygon	1362.087	FDA UDI	Class II	Active
Vygon	270.05	FDA UDI	Class II	Active
Vygon	AMS-9038CS-1	FDA UDI	Class II	Active
Vygon	AMS-8182-1	FDA UDI	Class II	Active
Vygon	AMS-9734	FDA UDI	Class II	Active
Vygon	1362.052	FDA UDI	Class II	Active
Vygon	1366.107	FDA UDI	Class II	Active
Premicath	1261.205G	FDA UDI	Class II	Active
Vygon	AMS-9021CP-1	FDA UDI	Class II	Active
Vygon	CLGY-2050	FDA UDI	Class II	Active
Vygon	AMS-968CP-1	FDA UDI	Class II	Active
Vygon	AMS-850TC	FDA UDI	Class I	Active
Vygon	SS-761B	FDA UDI	Class II	Active
Vygon	520.25	FDA UDI	Class II	Active
Vygon	2395.06	FDA UDI	Class II	Active
Vygon	AMS-9129CP	FDA UDI	Class I	Active
Vygon	1015.602	FDA UDI	Class II	Active
Vygon	AMS-373	FDA UDI	Class II	Active
Vygon	2395.09	FDA UDI	Class II	Active
Vygon	VYPL4S1001	FDA UDI	Class II	Active
Vygon	AMS-9788CP-1B	FDA UDI	Class I	Active
Vygon	1262.30N	FDA UDI	Class II	Active
Vygon	1015.012	FDA UDI	Class II	Active
Vygon	367.011	FDA UDI	Class I	Active
Vygon	VYPL4S1003	FDA UDI	Class II	Active
Vygon	364.062	FDA UDI	Class II	Active
Vygon	391.21	FDA UDI	Class II	Active
Vygon	5516.40	FDA UDI	Class II	Active
Vygon	AMS-9788CP-3	FDA UDI	Class I	Active
Vygon	2395.062G	FDA UDI	Class II	Active
Vygon	115.11	FDA UDI	Class II	Active
Vygon	310.09	FDA UDI	Class II	Unknown
Nutriline Twinflo	1252.232G	FDA UDI	Class II	Active
Vygon	AMS-428	FDA UDI	Class II	Active
Vygon	AMS-9093CP	FDA UDI	Class II	Active
Vygon	AMS-8268CS	FDA UDI	Class II	Active
Vygon	817.052	FDA UDI	Class II	Active
Vygon	AMS-895C	FDA UDI	Class II	Active
Vygon	AMS-9140-1	FDA UDI	Class II	Active
Vygon	AMS-395-1	FDA UDI	Class II	Active
Vygon	AMS-7658	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.