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FDA Medical Device Recalls (openFDA)

ConMed Corporation: STAT 2 I.V. Gravity Flow Needle-Free Controller Primary Administration Sets and Extension Sets (Catalog Numbers: (1) S2-12 N, STAT 2 Extension Set Gravity Flow Controller (Needle-Free), 12 length, (2) S2V-20 N, STAT 2 Primary Administration Set Gravity Flow Controller (Needle-Free), 20 Drops/ml, 84 length, and (3) S2V-60 N, STAT 2 Primary Administration Set Gravity Flow Controller (Needle-Free), 60 Drops/ml, 84 length) The STAT 2 Extension sets are for use in conjunction with commonly available I.V. administration sets for controlling the infusion of I.V. fluids into the human body. The STAT 2 Secondary and Primary Administration Sets are for use in attachment to an I.V. bag and patient catheter inserted into a vein to control the infusion of intravenous fluids into the human body. This is a disposable device with a sterile, nonpyrogenic fluid path.

Recall number
Z-0805-2018
Recalling firm
ConMed Corporation
Product
STAT 2 I.V. Gravity Flow Needle-Free Controller Primary Administration Sets and Extension Sets (Catalog Numbers: (1) S2-12 N, STAT 2 Extension Set Gravity Flow Controller (Needle-Free), 12 length, (2) S2V-20 N, STAT 2 Primary Administration Set Gravity Flow Controller (Needle-Free), 20 Drops/ml, 84 length, and (3) S2V-60 N, STAT 2 Primary Administration Set Gravity Flow Controller (Needle-Free), 60 Drops/ml, 84 length) The STAT 2 Extension sets are for use in conjunction with commonly available I.V. administration sets for controlling the infusion of I.V. fluids into the human body. The STAT 2 Secondary and Primary Administration Sets are for use in attachment to an I.V. bag and patient catheter inserted into a vein to control the infusion of intravenous fluids into the human body. This is a disposable device with a sterile, nonpyrogenic fluid path.
Status
Terminated
Initiated
2017-06-19
Posted
not on file
Terminated
2022-07-25
Reason
Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inconsistent flow rates.
Root cause
Nonconforming Material/Component
Action
The firm, ConMed, sent an "URGENT: DEVICE RECALL" letter dated 6/21/2017 to its domestic and foreign customers. The letter described the product, the problem and the actions to be taken. The customers were instructed NOT to use any STAT 2 I.V. Gravity Flow Controllers manufactured between April 27, 2012 and April 12, 2017; review your inventory for any of the devices listed on Attachment I; contact all of those departments within your facility and any other facilities within your organization that may have received affected products. It is imperative that all end users of these devices receive this notice and respond immediately; if you HAVE inventory of any of the devices listed, complete the Business Reply Form and return it with devices to: CONMED Corporation, 525 French Road, Utica, NY 13502 via UPS Account # W5Y243; if you DO NOT HAVE any affected devices complete and return the form by email: stat2@conmed.com; fax: Field Action Support Team at 315-624-3225 or US mail to CONMED Corporation, 525 French Road, Utica, NY 13502;Attn: Field Action Support Team. PLEASE DO NOT RETURN USED DEVICES. If you have any questions or requests, please dont hesitate to contact the Field Action Support Team at 1-800-448-6506, fax to 315-624-3225, or email stat2@conmed.com.
Quantity
1,612,440in total
Distribution
Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, Washington, DC, Puerto Rico, and countries of: Lebanon, Panama, Saudi Arabia, Germany, India, and Canada.
Lot, serial or model codes
Catalog Number, Manufacturing Date range, Lot Code range: (1) S2-12 N,4/27/12 - 4/12/17, 120427X - 201704124; (2) S2V-20 N, 4/27/12 - 11/7/17, 120427X - 201611074; and (3) S2V-60 N, 4/27/12 - 2/13/17, 120427X - 201702134
510(k) numbers
["K964844"]
PMA numbers
not on file
Product code
FPA
Firm FEI
3001451571
Firm city
Utica
Firm state
NY
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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