Reported Oct 24, 2012 · Terminated

***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Administration Set, REF…

MOOG Medical Devices Group

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: MOOG Medical Devices Group · 4314 Zevex Park Ln · Salt Lake City, UT · 84123-7881

Is this the product you have?

  • ***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Administration Set, REF 340-4165, Sterile EO, The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for the volumetric delivery of fluids used in Parenteral, Enteral, Epidural, Subcutaneous and Intravenous applications.
Lot codes and dates

3 of 3 products · 3 lot codes

Recalled lot codes, grouped by product number
Product CodeLot Number
340-4166
  • CF1022906
340-4128-V
  • CRF10082001
340-4165
  • CF1022905
Amount recalled
12,000 sets

Where it was sold

  • Nationwide
  • CA

Why it was recalled

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 Curlin Ambulatory Infusion Pumps. The lots associated with this recall were inadvertently omitted from the original recall which has since been terminated by

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 5, 2013 · Data as of Sep 19, 5:26 PM UTC

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