FreshRecalls

Medline Kits: recall status

⚠ Recall found. Medline Kits is named in 19 official recalls in our current data. Details and the official notices are below — act on the remedy in the official notice.

Brand
Medline Industries

Recalls naming this model

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1832-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1833-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1834-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1835-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1836-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1837-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1838-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1839-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1840-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1841-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1842-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1843-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1844-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1845-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1846-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1847-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1848-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1849-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Kits recall — Medline Industries, LP

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Official ID Z-1850-2026 · Official record ↗

See all Medline Industries recalls →

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Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 3:00 AM UTC.