# FDA recall Z-1157-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-01-04.

## Product

Medline Contro-Bulb Syringe, REF DYND20125; bulb irrigation syringe

## Reason for recall

Packaging material was updated for the Bulb Irrigation Syringe (DYND20125), and additional testing done at Medline Corporate indicated the potential for the sterile barrier to be breached during transportation. This only affects two lot numbers (96922110001 and 96923100001).

## Distribution

US, Nationwide

## Key facts

- **Recall number:** Z-1157-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-04
- **Report date:** 2024-09-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1157-2024

## Citation

> AI Analytics. FDA recall Z-1157-2024. Retrieved 2026-07-03 from https://api.ai-analytics.org/recall/Z-1157-2024. Source: US FDA. Licensed CC0.

---

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