Reported Sep 7, 2022 · Ongoing
NIM CONTACT EMG Endotracheal Tube, Part Numbers: a) REF 8229508 b) REF 8229507 c) REF 8229506
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 CONTACT EMG Endotracheal Tube
- Part Numbersa) REF 8229508 b) REF 8229507 c) REF 8229506
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 8229508006431697895790076300074586800763000882433UDI 00643169789579, 00763000745868, 00763000882433; ALL LOTS. 8229507006431697895620076300074585100763000882426UDI 00643169789562, 00763000745851, 00763000882426; ALL LOTS. 8229506006431697895550076300074584400763000882419UDI 00643169789555, 00763000745844, 00763000882419; ALL LOTS. - Amount recalled
- 81,555 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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