FDA recall record

Baxter Healthcare GEM(TM), FLOWCOUPLER(R), 3.0 mm, STERILE EO, Rx only, 1 FLOWCOUPLER, REF recall — FDA Z-1629-2016

Instructions for use booklet may puncture the outer Tyvek lid.

Class IIclassification
Z-1629-2016official record ID
May 18, 2016report date

Recall record at a glance

Official recordZ-1629-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBaxter Healthcare Corp.
Report dateMay 18, 2016
Recall initiation dateApr 21, 2016
Quantity707 units
LocationDeerfield, IL, United States

Official product description

GEM(TM), FLOWCOUPLER(R), 3.0 mm, STERILE EO, Rx only, 1 FLOWCOUPLER, REF GEM2754-FC Product Usage: The FlowCOUPLER Device is a single use, implantable device that is intended to be used in the end-to-end anastomosis of veins and arteries normally encountered in microsurgical and vascular reconstructive procedures. The FlowCOUPLER Device includes a pair of permanently implanted rings which secure the anastomosis and a removable Doppler probe that is press-fit onto one of the rings. When the FlowCOUPLER Device is used in conjunction with the FlowCOUPLER Monitor, the FlowCOUPLER System is intended to detect blood flow and confirm vessel patency intra-operatively and post-operatively at the anastomotic site.

Why the product was recalled

Instructions for use booklet may puncture the outer Tyvek lid.

Distribution information

Nationwide and Germany, Sweden, Netherlands, Israel, Denmark, United Kingdom, Canada

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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