Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
FDA Recall #Z-1758-2025 — Class I — April 17, 2025
Product Description
Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
Reason for Recall
Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
Recalling Firm
C.R. Bard Inc — Covington, GA
Classification
Class I — Reasonable probability of serious adverse health consequences or death.
Product Type
Devices
Product Quantity
N/A
Distribution
US: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA RI SC SD TN TX UT VA VT WA WI WV WY, Puerto Rico OUS: Singapore, Canada, Belgium, Ireland, Netherlands, South Africa, Sweden, United Kingdom
Code Information
All Lots within expiration/UDI: (01)00801741076831
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated