# FDA recall Z-1759-2025

> **C.R. Bard Inc** · Class I · device recall initiated 2025-04-17.

## 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.

## 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

## Key facts

- **Recall number:** Z-1759-2025
- **Recalling firm:** C.R. Bard Inc
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-17
- **Report date:** 2025-05-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Covington, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1759-2025

## Citation

> AI Analytics. FDA recall Z-1759-2025. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-1759-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*