Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
Reported: May 28, 2025 Initiated: April 17, 2025 #Z-1758-2025
Product Description
Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300
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.
Details
- Recalling Firm
- C.R. Bard Inc
- Units Affected
- 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
- Location
- Covington, GA
Frequently Asked Questions
What product was recalled? ▼
Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300. Recalled by C.R. Bard Inc. Units affected: N/A.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 28, 2025. Severity: Critical. Recall number: Z-1758-2025.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11