Reported Sep 7, 2022 · Ongoing
NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF 8229306
Medtronic Xomed, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.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
- Part Numbersa) REF 8229308 b) REF 8229307 c) REF 8229306
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 8229308006431697895480076300074583700763000882402UDI 00643169789548, 00763000745837, 00763000882402; ALL LOTS. 8229307006431697895310076300074582000763000882396UDI 00643169789531, 00763000745820, 00763000882396; ALL LOTS. 8229306006431697895240076300074581300763000882389UDI, 00643169789524, 00763000745813, 00763000882389; ALL LOTS. - Amount recalled
- 1,133,612 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Stop using this product now
The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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