FDA recall record

TELEFLEX-MORRISVILLE Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use recall — FDA Z-0009-2020

Device vented gas below the stated pressure.

Class Iclassification
Z-0009-2020official record ID
Nov 13, 2019report date

Recall record at a glance

Official recordZ-0009-2020
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmTELEFLEX-MORRISVILLE
Report dateNov 13, 2019
Recall initiation dateJun 14, 2019
Quantity9,312 each
LocationMorrisville, NC, United States

Official product description

Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.

Why the product was recalled

Device vented gas below the stated pressure.

Distribution information

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

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.