Bard¿ Blakemore Esophageal-Nasogastric Tube recall
Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
Why was Bard¿ Blakemore Esophageal-Nasogastric Tube recalled?
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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All Lots within expiration/UDI: (01)00801741076831
- Product
- Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
- Recalling firm
- C.R. Bard Inc
- 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
- Recall date
- May 28, 2025
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)