Reported Apr 25, 2018 · Terminated

Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in…

Teleflex Medical Europe Ltd.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Teleflex Medical Europe Ltd · Ida Business Park · Athlone · N/A

Is this the product you have?

  • Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644
  • QTY 50 Product Usagefor use in respiratory and anesthesia circuits to connect two or more components of a breathing system
Lot codes and dates
  • Lot Numbers

    77 of 77 codes

    • 74D1501706
    • 74K1502092
    • 74F1600367
    • 74J1600117
    • 74L1601916
    • 74C1701733
    • 74F1700707
    • 74D1501731
    • 74K1502045
    • 74F1601072
    • 74J1601101
    • 74M1600284
    • 74C1702365
    • 74F1701866
    • 74G1500664
    • 74M1501145
    • 74F1601874
    • 74J1601563
    • 74M1601685
    • 74D1700030
    • 74F1702612
    • 74G1500663
    • 74A1601936
    • 74F1602470
    • 74J1602238
    • 74A1700107
    • 74D1700363
    • 74G1700034
    • 74G1502412
    • 74B1600334
    • 74G1600466
    • 74K1600148
    • 74A1701335
    • 74D1701038
    • 74G1700488
    • 74H1500466
    • 74C1600162
    • 74H1600217
    • 74K1600287
    • 74A1701403
    • 74D1701507
    • 74G1701144
    • 74H1500189
    • 74D1601420
    • 74H1600516
    • 74K1601020
    • 74A1702060
    • 74E1700450
    • 74G1702002
    • 74H1501260
    • 74D1601965
    • 74H1601371
    • 74K1601924
    • 74A1702874
    • 74E1700965
    • 74H1700127
    • 74H1501971
    • 74E1600800
    • 74H1601372
    • 74L1600063
Amount recalled
103910 units

Where it was sold

  • Nationwide
  • CA

Why it was recalled

These one-way valves may disconnect at the joint between the two components that make up the device, which would cause an interruption of ventilation to the patient.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 4, 2021 · Data as of Sep 19, 5:31 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.