C.R. Bard Inc 2025-05-28 Health critical FDA
Health · FDA · Recall #FDA-Z-1759-2025
Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740 Recall
Issued May 28, 2025 · C.R. Bard Inc
In May 2025, C.R. Bard Inc recalled the Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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 you should do
- 1 Stop using Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact C.R. Bard Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- C.R. Bard Inc
- Category
- Health
- Recall date
- May 28, 2025
- Units affected
- Not reported
- Sold at
- 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
- Recall number
- FDA-Z-1759-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- C.R. Bard Inc has 6 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.