Reported Jan 4, 2017 · Terminated
NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.
Medtronic Xomed, Inc.
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: Medtronic Xomed, Inc. · 6743 Southpoint Dr N · Jacksonville, FL · 32216-6218
Is this the product you have?
- NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.
- Lot codes and dates
3 of 3 products
Products covered by this recall # Product as published 1 All lots distributed since May 2012. Catalog Ref No. (reinforced standard tubes) 82-29306, 82-29307, & 82-29308 2 Catalog Ref No. (reinforced standard tubes, Japan) 8229306J, 8229307J, & 8229308J 3 Catalot Ref No. (reinforced contact tubes) 8229506, 8229507, & 8229508 - Amount recalled
- 3752
Where it was sold
- Nationwide
- PR
Why it was recalled
Wire in tubing can become exposed, posing potential harm to the intubated patient.
This product could cause temporary or reversible health problems — stop using it.
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