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STAT 2 Flow Controller recallZ-2620-2014 · ICU Medical, Inc. · initiated Aug 19, 2014

Class I Terminated All recalls posted in September 2014

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from ICU Medical, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

ICU is recalling the ConMed Stat 2 flow controller because it may deliver a significantly higher flow rate than was intended.

FDA root cause category: Nonconforming Material/Component

What the company is doing

ICU Medical sent an Urgent Medical Device Recall letter dated August 19, 2014 to all affected customers. The letter identified the affected product, problems identified and the actions to be taken. Customers were instructed to complete the recall response form and fax to ICU Medical at (801) 264-1755 or by email: [email protected]. Customers with questions or require assistance relating to this recall were instructed to contact ICU Customer Service Monday through Friday between the hours of 8:30 AM and 4:00 PM Pacific time: 866-829-9025 and select option 8, or e-mail the following address: [email protected]. For questions regarding this recall call 801-264-1732.

Recall details

Recall number
Z-2620-2014
Recall class
Class I (most serious)
Status
Terminated
Initiated by the company
Aug 19, 2014
Posted by the FDA
Sep 19, 2014
Recalling firm
ICU Medical, Inc.
Quantity
1250 units
Product code
FMG
FDA submissions
K964435
Distribution
Worldwide Distribution - US (nationwide) in the state of WA, OR and the country of South Africa.

Product description

STAT 2 Flow Controller; 80" (203 cm) Appx 14.8 mL, 60 Drop Primary Set w/2 Clave, STAT 2 Flow Controller, Rotating Luer, Item No. 011-C9802. Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are provided sterile.

Code information (models, lots, serial numbers)

Lot # 2768417

Other devices under the same FDA submission

563 devices cleared under K964435 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.

Other products in the same recall event

The FDA groups related products into one recall event (event 69088).

Sources and updates

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