Reported Dec 31, 2014 · Terminated
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 mm, Distributed by Kimberly Clark Global Sales, LLC.…
Halyard Health
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: Halyard Health · 1400 Holcomb Bridge Rd · Roswell, GA · 30076-2190
Is this the product you have?
- KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.
- Lot codes and dates
- Product Code13220
- Lot numbers
AA3213AA3227AA3227V01AA3245AA3245V02AA3253V02AA3269V01AA3274V01AA4038AA4038V03AA4038V04AA4038V06AA4062AA4062V01AA4104V02AA4111V01AA4113V01AA4134V01 & AA4146V01AA4146V04AA4174V01
- Amount recalled
- 250 cases (10 tubes per case)
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Stop using this product now
The cuff inflation line may detach from the endotracheal tube during use.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
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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