Medline Kits: recall status ⚠ Recalls found. Medline Kits is named in 19 official recalls in our current data:
FDA Class II recall Z-1832-2026 — The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.FDA Class II recall Z-1833-2026 — The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.FDA Class II recall Z-1834-2026 — The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.And 16 more listed below. Source checks: September 7, 2026 at 6:00 AM UTC (oldest successful check).
Sources, dates and coverage limits We collect recent notices on a six-hour schedule using a rolling 90-day source request. Older retained records may also appear. This is a recall index, not a catalogue of all products or a complete recall history.
CPSC: stored recall dates April 30, 2026 to September 3, 2026. NHTSA: stored recall dates April 24, 2026 to September 1, 2026. FDA: stored recall dates April 29, 2026 to August 19, 2026. USDA FSIS is not aggregated here. Check USDA meat, poultry and processed egg notices . EPA and U.S. Coast Guard are not aggregated. Source delays and missing identifiers can prevent a match.
Brand Medline Industries Recalls naming this model FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1832-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1833-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1834-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1835-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1836-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1837-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1838-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1839-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1840-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1841-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1842-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1843-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1844-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1845-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1846-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1847-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1848-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1849-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries
Affected product: Medline Kits
Official ID Z-1850-2026 ·
Official record ↗
See all Medline Industries recalls →
Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.