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TELEFLEX-MORRISVILLE recalls Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.
Recalled November 13, 2019 · FDA recall Z-0009-2020 · TELEFLEX-MORRISVILLE
Hazard
Device vented gas below the stated pressure. · FDA Class I
Units
9,312 each
Sold at
US nationwide distribution. AL, CA, CO, CT, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TX, VA, WA and WY
Description
Device vented gas below the stated pressure.
Product
Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.
Manufacturer(s)
TELEFLEX-MORRISVILLE
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →