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# Teleflex Class 1 Recall of Ventilator Manifold
- URL: https://www.fdaweb.com/teleflex-class-1-recall-of-ventilator-manifold/
- Published: 2019-11-08T12:00:00.000Z
- Updated: 2026-09-14T15:52:30.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5145466

Teleflex has begun a Class 1 recall of its Babi.Plus 12.5 cm H2O Pressure Relief Manifold, which is used with its ventilators, because the device’s vented gas is below the stated pressure. A company communication to customers instructs them to quarantine affected products, according to a [recall notice](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=173770&ref=fdaweb.com). The company says about 9,300 devices are currently in distribution.