FDA Device recall Z-1759-2025
Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740
- FDA Device
- Class I
- ongoing
- Published 2025-05-28
On 2025-05-28 the FDA classified a Class I recall of Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740 by C R Bard, citing 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 ballo….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1759-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-04-17 |
| Published | 2025-05-28 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | C R Bard |
| Distribution | 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, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
Product
Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740
Reason
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.
Identifiers
| code_info | All Lots within expiration/UDI: (01)00801741076848 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1759-2025%22
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