Bard¿ Single Intragastric Linton Balloon Tube — Class I medical device recall Z-1759-2025
Ongoing recall by C.R. Bard Inc, reported 2025-05-28, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the
| Recall number | Z-1759-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | C.R. Bard Inc, Covington, GA, United States |
| Recall initiated | 2025-04-17 |
| Classified | 2025-05-20 |
| Reported by FDA | 2025-05-28 |
| Distributed | 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 |
| Countries outside the US | BE, CA, GB, IE, NL, SE, SG, ZA |
| UPC / GTIN / UDI-DI | 00801741076848 |
| Model numbers | 0092740 |
Product
Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1759-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.