# FDA recall Z-1876-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class I · device recall initiated 2024-02-26.

## Product

Medline Sub-G Endotracheal Tube with Subglottic Suctioning:    (1) REF DYNJ18860, Polyurethane Cuff 6.0 mm ID;  (2) REF DYNJ18865, Polyurethane Cuff 6.5 mm ID;  (3) REF DYNJ18870, Polyurethane Cuff 7.0 mm ID;  (4) REF DYNJ18875, Polyurethane Cuff 7.5 mm ID;  (5) REF DYNJ18880, Polyurethane Cuff 8.0 mm ID; and  (6) REF DYNJ18885, Polyurethane Cuff 8.5 mm ID.    Medline SubG Endotracheal Tube with Subglottic Suctioning packaged into the following convenience kits:    (1) Medline Intubation Kit - Drawer 3, Reorder No. ACC010502, containing 6.0, 7.0, 7.5, 8.0, and 8.5 sizes subglottic cuff, 6 kits/case;  (2) Medline Intubation Tube - Drawer 3, Reorder No. ACC010527, containing 6.0, 7.0, 7.5, 8.0, and 8.5 sizes subglottic cuff, 6 kits/case;  (3) Medline Adult Intubation, Reorder No. ACC010540, containing 8.5 size subglottic cuff, 3 kits/case;  (4) Medline Adult Intubation, Reorder No. ACC010540A, containing 8.5 size subglottic cuff, 3 kits/case;  (5) Medline Airway Kit - Drawer 3, Reorder N

## Reason for recall

Complaints have been received that the device inflation tube detached and/or tore from the main tube, resulting in potential moisture buildup, loss of pressure, or inability to inflate.  There were also reports the suction pump is difficult to connect or detaches during use.

## Distribution

Distribution was nationwide.  There was government/military distributon.  Foreign distribution was made to San Salvador and United Arab Emirates.

## Key facts

- **Recall number:** Z-1876-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-26
- **Report date:** 2024-06-05

- **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-1876-2024

## Citation

> AI Analytics. FDA recall Z-1876-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1876-2024. Source: US FDA. Licensed CC0.

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