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ZEVEX INTERNATIONAL, INC.

Last updated May 24, 2026

What ZEVEX INTERNATIONAL, INC. makes

The company manufactures single-use electric infusion pump administration sets, reusable personal device holders, and enteral feeding bags and bottles with screw caps and EnFit connectors. It also produces enteral feeding pumps, portable rechargeable battery packs, voltage-converting power supplies, and patient-controlled analgesia infusion pumps. Medical device service rail clamps are included in its product range.

All listed devices fall under Class II regulatory classification and are registered in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
Address: —
Website: moog.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 800-970-2337
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 612746933

Catalogue (111)

Page 3 of 3

Device	Model / Reference	Registries	Class	Status
Infinity	1	FDA UDI	Class II	Unknown
Curlin Administration Set	340-4170	FDA UDI	Class II	Active
Curlin Administration Set	340-4130-V	FDA UDI	Class II	Active
GR 1200 mL Feeding Bag Set with Enfit Connector	GR1200-E	FDA UDI	Class II	Active
Curlin Administration Set	340-4144	FDA UDI	Class II	Active
Curlin Administration Set	340-4164	FDA UDI	Class II	Active
Curlin	1	FDA UDI	Class II	Unknown
Infinity	Infinity Waist Pack, Black	FDA UDI	Class II	Active
Curlin	1	FDA UDI	Class II	Unknown
Infinity	Infinity Super Mini Backpack, Black	FDA UDI	Class II	Active
Infinity	PCK2001	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (27)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Zevex International, Inc. has 27 recall records initiated between December 18, 2008, and February 28, 2011, all marked as terminated. The recalls involved issues such as defects in tubing that could trigger false Air-In-Line warnings, infusion pumps displaying false error codes rendering them inoperable until recovery, and enteral feeding pumps failing to deliver fluid accurately, potentially causing under-infusion or over-infusion.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Feb 28, 2011	Z-1869-2011	—	terminated	Infusion pumps may exhibit false error codes which render the device inoperable until a recovery process is performed.
Feb 28, 2011	Z-1870-2011	—	terminated	Infusion pumps may exhibit false error codes which render the device inoperable until a recovery process is performed.
Feb 28, 2011	Z-1867-2011	—	terminated	Infusion pumps may exhibit false error codes which render the device inoperable until a recovery process is performed.
Feb 28, 2011	Z-1868-2011	—	terminated	Infusion pumps may exhibit false error codes which render the device inoperable until a recovery process is performed.
Jan 24, 2011	Z-1453-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-2808-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1446-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1456-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1448-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1439-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1447-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1455-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1445-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1450-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1452-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1454-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1451-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1443-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1444-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1440-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1449-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-2809-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1442-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-1441-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Jan 24, 2011	Z-2807-2011	—	terminated	Defect in tubing may trigger false Air-In-Line warning.
Dec 18, 2008	Z-2113-2009	—	terminated	Enteral feeding pumps may not accurately deliver fluid, potentially under-infusing or over-infusing.
Dec 18, 2008	Z-2112-2009	—	terminated	Enteral feeding pumps may not accurately deliver fluid, potentially under-infusing or over-infusing.