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[Recalled] VentStar Anesthesia (N) 180, MP00333 — Glued connections of the breathing circuit can become loose before or during ve… | FDA 2023-04-17

recall fda device united-states

Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.

Recall details

ProductVentStar Anesthesia (N) 180, MP00333
Brand / manufacturerDraeger Medical, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1447-2023
Country of noticeUnited States
Risk levelClass I
Hazard typerecall
Notice date17 April 2023
EAN / barcode04048675422198

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.

This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).

Read the full official notice →

Related recalls from Draeger Medical, Inc.

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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