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Teleflex Medical Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column - safety alert

Official notice

23 Dec 2015

Last checked

23 Dec 2015

Medium riskFDA

An official FDA notice concerns Teleflex Medical Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column - safety alert. An official FDA notice concerns Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2015-12-23. Lots: 02K1300128. Recall numbers: Z-0419-2016. Check the official notice for the complete list. Published 2015-12-23.

What to do now

The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.

Units affected

2,600

Recall number

Z-0419-2016

Official notice

2015-12-23

The hazard

An official FDA notice concerns Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2015-12-23. Lots: 02K1300128. Recall numbers: Z-0419-2016. Check the official notice for the complete list.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Lots

02K1300128

Event Ids

72731

Recall Numbers

Z-0419-2016

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Affected products

Product 1

Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column

Units affected

2,600

Risk / hazard

An official FDA notice concerns Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2015-12-23. Lots: 02K1300128. Recall numbers: Z-0419-2016. Check the official notice for the complete list.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States · NC · Durham

Affected area 1

US · United States · NC · Durham

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Teleflex Medical. Contact: Teleflex Medical.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-0419-2016

Event id

72731

Units affected

2,600

Status

terminated

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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