Data Foundry

Medical device recalls 2025

Bard Blakemore Esophageal-Nasogastric Tube — Class I medical device recall Z-1756-2025

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 numberZ-1756-2025
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmC.R. Bard Inc, Covington, GA, United States
Recall initiated2025-04-17
Classified2025-05-20
Reported by FDA2025-05-28
DistributedAK, 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 USBE, CA, GB, IE, NL, SE, SG, ZA
UPC / GTIN / UDI-DI00801741076800
Model numbers0092100

Product

Bard Blakemore Esophageal-Nasogastric Tube (Adult) REF: 0092100

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-1756-2025. 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.