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
74D150170674K150209274F160036774J160011774L160191674C170173374F170070774D150173174K150204574F160107274J160110174M160028474C170236574F170186674G150066474M150114574F160187474J160156374M160168574D170003074F170261274G150066374A160193674F160247074J160223874A170010774D170036374G170003474G150241274B160033474G160046674K160014874A170133574D170103874G170048874H150046674C160016274H160021774K160028774A170140374D170150774G170114474H150018974D160142074H160051674K160102074A170206074E170045074G170200274H150126074D160196574H160137174K160192474A170287474E170096574H170012774H150197174E160080074H160137274L1600063
- Lot Numbers
- 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.
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