Exact FDA event identifier

Event 78573

6 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: November 10, 2017
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Zevex Incorporated (dba Moog Medical Medical Devices Group)

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

6 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 6

MOOG Curlin Infusion Administration Set, Ref 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag Spike, packaged 20/box, for use with the MOOG Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.

Z-0697-2018

Recall number: Z-0697-2018
Initiated: November 10, 2017
Classification: Class II
Status: Terminated
Recalling firm: Zevex Incorporated (dba Moog Medical Medical Devices Group)
Quantity: 56,244/20 administration set cases

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0

Particulate

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Particulate found on the Curlin spike.

Code information

UDI 38148440000396, Lot/serial numbers: CF1514703, CF1514702, CF1514702, CF1514701, CF1514702, CF1517405, CF1517406, CF1518301, CF1518302, CF1518303, CF1518301, CF1521101, CF1521103, CF1521102, CF1521701, CF1522306, CF1522308, CF1522307, CF1523312, CF1524407, CF1524407, CF1525101, CF1524407, CF1525103, CF1525102, CF1526505, CF1526506, CF1527307, CF1527306, CF1528011, CF1528607, CF1528606, CF1529306, CF1529307, CF1530106, CF1530707, CF1530706, CF1530706, CF1530705, CF1530706, CF1530707, CF1530706, CF1530707, CF1532102, CF1531406, CF1532102, CF1531405, CF1532975, CF1532976, CF1532976, CF1532976, CF1532976, CF1535001, CF1533504, CF1534902, CF1535666, CF1600507, CF1600508, CF1601203, CF1601903, CF1602604, CF1603304, CF1604704, CF1605406, CF1606104, CF1607504, CF1610405, CF1611003, CF1612404, CF1613105, CF1613804, CF1615209, CF1616608, and CF1616608.

Distribution pattern

Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.

device · product 2 of 6

MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Needleless Injection Port (Positive Pressure), packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.

Z-0698-2018

Recall number: Z-0698-2018
Initiated: November 10, 2017
Classification: Class II
Status: Terminated
Recalling firm: Zevex Incorporated (dba Moog Medical Medical Devices Group)
Quantity: 756/20-administration set cases

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0

Particulate

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Particulate found on the Curlin spike.

Code information

UDI 38148440000488, Lot/serial numbers: CF1519507, CF1522502, CF1524406, and CF1528008.

Distribution pattern

Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.

device · product 3 of 6

MOOG Curlin Infusion Administration Set, Ref 340-4134, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and Y-Site with Check Valve, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.

Z-0699-2018

Recall number: Z-0699-2018
Initiated: November 10, 2017
Classification: Class II
Status: Terminated
Recalling firm: Zevex Incorporated (dba Moog Medical Medical Devices Group)
Quantity: 2,497/20-administration set cases

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0

Particulate

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Particulate found on the Curlin spike.

Code information

UDI 38148440000495, Lot/serial numbers: CF1518304, CF1521104, CF1524301, CF1523803, CF1528603, and CF1613101.

Distribution pattern

Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.

device · product 4 of 6

MOOG Curlin Infusion Administration Set, Ref 340-4166, Non-DEHP Microbore Tubing with Non-Vented Spike, Anti-Siphon Valve included for Free Flow Protection, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.

Z-0700-2018

Recall number: Z-0700-2018
Initiated: November 10, 2017
Classification: Class II
Status: Terminated
Recalling firm: Zevex Incorporated (dba Moog Medical Medical Devices Group)
Quantity: 7,979/20-administration set cases

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0

Particulate

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Particulate found on the Curlin spike.

Code information

UDI 38148440000563, Lot/serial numbers: CF1515305, CF1519505, CF1523004, CF1524405, CF1529201, CF1528602, CF1532105, CF1601204, CF1604701, CF1605403, CF1609005, CF1609604, and CF1614732.

Distribution pattern

Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.

device · product 5 of 6

MOOG Curlin Infusion Administration Set, Ref 340-4168, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Female Luer Y-Site with Check Valve, Anti-Siphon Valve included for Free Flow Protection, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.

Z-0701-2018

Recall number: Z-0701-2018
Initiated: November 10, 2017
Classification: Class II
Status: Terminated
Recalling firm: Zevex Incorporated (dba Moog Medical Medical Devices Group)
Quantity: 2,417/20-administration set cases

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0

Particulate

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Particulate found on the Curlin spike.

Code information

UDI 38148440000587, Lot/serial numbers: CF1517404, CF1519506, CF1521211, CF1519506, CF1522501, CF1526503, CF1530704, CF1530704, CF1530704, CF1611001, and CF1618152.

Distribution pattern

Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.

device · product 6 of 6

MOOG Curlin Infusion Administration Set, Ref 340-4169, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Ultrasite Needleless Injection Port (Positive Pressure), Anti-Siphon Valve included for Free Flow Protection, packaged 20/box, for use with the Moog Curlin Ambulatory Volumetric Infusion Pump, RX, Sterile. Product Usage: Administration set to be used with the Moog Curlin infusion Pump. The pump can be used for intravenous, intra-arterial, epidural, subcutaneous, or enteral infusions.

Z-0702-2018

Recall number: Z-0702-2018
Initiated: November 10, 2017
Classification: Class II
Status: Terminated
Recalling firm: Zevex Incorporated (dba Moog Medical Medical Devices Group)
Quantity: 785/20-administration set cases

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0

Particulate

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Particulate found on the Curlin spike.

Code information

UDI 38148440000594, Lot/serial numbers: CF1520208, CF1522301, and CF1532971.

Distribution pattern

Distribution was nationwide. There was government and military distribution. Foreign distribution was made to Canada, Saudi Arabia, Turkey, Croatia, United Arab Emirates, and Australia.