| Class 2 Device Recall STAT 2 I.V. Gravity Flow Controller and STAT 2 Primary, Secondary Administration and Extension set | |
Date Initiated by Firm | June 19, 2017 |
Create Date | February 28, 2018 |
Recall Status1 |
Terminated 3 on July 25, 2022 |
Recall Number | Z-0804-2018 |
Recall Event ID |
79129 |
510(K)Number | K905498 |
Product Classification |
Controller, infusion, intravascular, electronic - Product Code LDR
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Product | STAT 2 I.V. Gravity Flow Controller and STAT 2 Primary, Secondary Administration Sets and Extension Sets (Catalog Numbers: (1) S2, STAT 2 I.V. Controller, (2) S2-12, STAT 2 Extension Set Gravity Flow Controller, 12 length, (3) S2-20 MD, STAT 2 Secondary Set Gravity Flow Controller, 20 Drops/ml, 13 length, (4) S2V-20, STAT 2 Primary Administration Set Gravity Flow Controller, 20 Drops/ml, 84 length, and (5) S2V-60, STAT 2 Primary Administration Set Gravity Flow Controller, 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. |
Code Information |
Catalog Number, Manufacturing Date range, Lot Code range: (1) S2, 4/27/12 - 2/1/17, 120427X - 201702014; (2) S2-12, 4/27/12 - 3/13/17, 120427X - 201703134; (3) S2-20 MD, 4/27/12 - 1/2/17, 120427X - 201701024; (4) S2V-20, 4/27/12 - 4/7/17, 120427X - 201704074; and (5) S2V-60, 4/27/12 - 3/16/17, 120427X - 201703164 |
Recalling Firm/ Manufacturer |
ConMed Corporation 525 French Rd Utica NY 13502-5945
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For Additional Information Contact | M. Patricia Cotter 315-624-3533 |
Manufacturer Reason for Recall | Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or inconsistent flow rates. |
FDA Determined Cause 2 | 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 in Commerce | 1,612,440 in 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. |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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510(K) Database | 510(K)s with Product Code = LDR
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