HUDSON RCI COMFORT FLO Corrugated Humidification System, REF 2415, humidifier nebulizer kit
FDA Recall Z-1112-2020 · Posted 2020-02-07
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Recalling FirmTELEFLEX MEDICAL INC
Recall StatusTerminated
Product CodeBTT
Date Initiated2019-12-13
Date Terminated2024-04-30
Product Quantity30566 devices
Reason for Recall
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column during high flow oxygen therapy.
Firm Action
The firm initiated the recall by letter on 12/13/2019. The firm is seeking the return of the product.
The firm requested the following actions be taken:
"1. If you have affected stock, immediately identify all patients that are currently exposed to use of this product, discontinue use and quarantine any products with the product codes and lot numbers listed above.
2. To acknowledge receipt of this Urgent Medical Device Recall Notice or to return product, complete the enclosed Recall Acknowledgement Form and fax it to 1-855-419-8507, Attn: Customer Service or email to [email protected]. This will allow us to document the amount of product you have on hand for return. A customer service representative will contact you with a Return Goods Authorization (RGA) Number and will provide instructions for the return of products to Teleflex Medical.
3. If you have no affected stock, please complete the enclosed Recall Acknowledgment Form and fax it to 1-855-419-8507, Attn: Customer Service or email to [email protected]. This will allow us to document your receipt of this letter.
If you have any other questions, feel free to contact your local sales representative or Customer Service at 1-866-396-2111.
Root Cause
Device Design
Distribution Pattern
nationwide
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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