Curlin Administration Set

30 catalogue numbers from 340-4130, listed by Zevex, Inc., United States, under Pump, Infusion. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
30catalogue numbers in this listing
2510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Shanghai (2), Guangdong (2), Jiangsu (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FRN
Manufacturer City Province Registered as Device types
Sanmina Kunshan Jiangsu Contract manufacturer 15
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
JDI Electronics Factory Dongguan Guangdong Contract manufacturer 7
Zyno Electric & Machinery Ltd, Shanghai Shanghai Shanghai Contract manufacturer 1
Sterigenics Shanghai E Beam Ltd. Shanghai Shanghai Contract manufacturer 14

Record

Regulatory record for Curlin Administration Set
Listed by Zevex, Inc., United States
FDA product code FRN
Device type Pump, Infusion
Device class Class 2
Regulation 21 CFR 880.5725
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
Record published 2016-10-22
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date
Packaging Pack of 20

Catalogue Numbers

Catalogue numbers for Curlin Administration Set
Catalogue number Size Status
340-4130 In distribution
340-4173 In distribution
340-4137 In distribution
340-4133 In distribution
340-4174 In distribution
340-4128-V In distribution
340-4176 In distribution
340-4175 In distribution
340-4171 In distribution
340-4167 In distribution
340-4144 In distribution
340-4163 In distribution
340-4111 In distribution
340-4115 In distribution
340-4128 In distribution
340-4134 In distribution
340-4162 In distribution
340-4127 In distribution
340-4177 In distribution
340-4130-V In distribution
340-4165 In distribution
340-4126 In distribution
340-4119 In distribution
340-4164 In distribution
340-4166 In distribution
340-4169 In distribution
340-4168 In distribution
340-4114 In distribution
340-4170 In distribution
340-4172 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Port Access Infusion SET Sb-Kawasumi Laboratories, Inc. 76
Cadd ICU Medical, Inc 56
Flow Control Tubing GO Medical Industries PTY. Ltd. 39
ambIT Summit Medical Products, Inc. 27
Beeline motIV Rex Pj Tech LLC 24
RMS Precision Flow Rate TubingTM Repro-Med Systems, Inc. 24
Medfusion ICU Medical, Inc 24
Volumat™ Line Fresenius Kabi AB 24
Outlook® B. Braun Medical Inc. 21
Alaris CareFusion 303, Inc 19
Alpha Source Battery Alpha Source Inc. 17
Plum ICU Medical, Inc 14

Showing 12 of 191. All products under Pump, Infusion

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242660 2024-10-03
K232793 2024-05-17

Recalls Naming This Product

8 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Curlin Administration Set
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Zevex, Inc. UDI-DI 2019-02-27 Class II Nonconforming Material/Component Administration sets leaked at the filter. 569/20-set caess 2021-04-28
Zevex, Inc. UDI-DI 2019-02-27 Class II Nonconforming Material/Component Administration sets leaked at the filter. 756/20-set cases 2021-04-28
Zevex, Inc. UDI-DI 2017-11-10 Class II Nonconforming Material/Component Particulate found on the Curlin spike. 56,244/20 administration set cases 2018-12-12
Zevex, Inc. UDI-DI 2017-11-10 Class II Nonconforming Material/Component Particulate found on the Curlin spike. 756/20-administration set cases 2018-12-12
Zevex, Inc. UDI-DI 2017-11-10 Class II Nonconforming Material/Component Particulate found on the Curlin spike. 2,497/20-administration set cases 2018-12-12
Zevex, Inc. UDI-DI 2017-11-10 Class II Nonconforming Material/Component Particulate found on the Curlin spike. 7,979/20-administration set cases 2018-12-12
Zevex, Inc. UDI-DI 2017-11-10 Class II Nonconforming Material/Component Particulate found on the Curlin spike. 2,417/20-administration set cases 2018-12-12
Zevex, Inc. UDI-DI 2017-11-10 Class II Nonconforming Material/Component Particulate found on the Curlin spike. 785/20-administration set cases 2018-12-12

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2015-12-23 Class II Process control Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps manufactured or serviced by MMDG between March 18, 2015 and November 6, 2015 because the master pumps used to calibrate them were out of tolerance and may cause an over deliv 11,472 2017-02-21
2012-09-26 Class II Process control This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which was related to customers reporting unclearable Air-In-Line alarm with specific lot numbers of Curlin Administration Sets used with 12,000 sets 2013-04-05
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 204 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 520 (never distributed – all in Moog’s possession) 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 11,628 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 77 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 814 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 1480 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 104 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 932 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 204 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 204 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 406 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 2652 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 2 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 125 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 816 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 18,494 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 4341 2012-07-26
2012-03-20 Not classified Nonconforming Material/Component Ambulatory administration sets used with the Curlin Ambulatory Pumps including the 4000 CMS Ambulatory Pump, 6000 CMS Ambulatory Pump and the Pain Smart IOD Ambulatory Pump may leak during use. 693 2012-07-26
2011-02-28 Not classified Software design Infusion pumps may exhibit false error codes which render the device inoperable until a recovery process is performed. 918 units 2012-08-06
2011-02-28 Not classified Software design Infusion pumps may exhibit false error codes which render the device inoperable until a recovery process is performed. 11,902 units 2012-08-06
2011-02-28 Not classified Software design Infusion pumps may exhibit false error codes which render the device inoperable until a recovery process is performed. 3,407 units 2012-08-06
2011-02-28 Not classified Software design Infusion pumps may exhibit false error codes which render the device inoperable until a recovery process is performed. 2079 units 2012-08-06
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 8,080 units 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 178,820 units (US), 220 units (INTL) 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 840 units 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 4500 Units (US),. 140 units (INTL) 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 12,400 units (US) 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 179,460 units (US), 960 units (INTL) 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 2,020 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 51,400 units (US), 1600 units (INTL) 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 1320 units (US) 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 17,120 units (US), 240 units (INTL) 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 185,360 units (US), 140 units (INTL) 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 4,060 units (US) 2011-09-27
2011-01-24 Not classified Process control Defect in tubing may trigger false Air-In-Line warning. 222,900 units (US) 2011-09-27

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer