NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.
Reported: January 4, 2017 Initiated: June 28, 2016 #Z-0901-2017
Product Description
NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.
Reason for Recall
Wire in tubing can become exposed, posing potential harm to the intubated patient.
Details
- Recalling Firm
- Medtronic Xomed, Inc.
- Units Affected
- 3752
- Distribution
- Worldwide Distribution - Nationwide Distribution including US Virgin Island and Puerto Rico , and to the countries of :Japan, Korea, China, Canada, Dominican Republic, Colombia, Chile, Costa Rica, Bahamas, Peru, Panama, Mexico, Argentina, Ecuador, Brazil, Trinidad and Tobago, Hong Kong, Taiwan, United Kingdom, Netherlands, Sri Lanka, Austria, Italy, Germany, United Arab Emirates, Saudi Arabia, Kuwait, France, Belgium, Oman, Ireland, Azerbaijan, India, Spain, Portugal, Luxembourg, Switzerland, Russian Federation, Austria, Greece, Cyprus, Portugal, India, Algeria, Iceland, Iran, Denmark, Hungary, Czech Republic, Ukraine, Turkey, Croatia, Israel, Norway, Oman, Sweden, Libya, Finland, Spain, Portugal, Algeria, Morocco, Poland, Canada, Malaysia, Singapore, Australia, and New Zealand
- Location
- Jacksonville, FL
Frequently Asked Questions
What product was recalled? ▼
NIM EMG Endotracheal Tube, 6.0 mm I.D. x 8.8 mm O.D. (27 FR), Reinforced, Sterile, Rx only. Individually packaged.. Recalled by Medtronic Xomed, Inc.. Units affected: 3752.
Why was this product recalled? ▼
Wire in tubing can become exposed, posing potential harm to the intubated patient.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 4, 2017. Severity: Moderate. Recall number: Z-0901-2017.
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