1,617 recent medical device recalls in our current data. Showing 1,601–1,617, newest first.
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1842-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1841-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1840-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1839-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1838-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1837-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1836-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1835-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1834-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1833-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Kits recall status
Official ID Z-1832-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Syringes recall status
Official ID Z-1831-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Namic Syringes recall status
Official ID Z-1830-2026 · Official record ↗
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Company / brand: Medline Industries recalls
Affected product: Medline Namic Guidewires recall status
Official ID Z-1829-2026 · Official record ↗
Software issue that renders the touch screen unresponsive.
Company / brand: Integra LifeSciences (NeuroSciences) recalls
Affected product: CUSA Clarity C7000 Console recall status
Official ID Z-1828-2026 · Official record ↗
In some foreseeable use conditions, the products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for …
Company / brand: Uvlizer c/o RAIS INTERNATIONAL recalls
Affected product: The product is a handheld ultraviolet-C germicidal wand and contains a combination of five recall status
Official ID Z-1808-2026 · Official record ↗
In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for …
Company / brand: Uvlizer c/o RAIS INTERNATIONAL recalls
Affected product: The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure merc recall status
Official ID Z-1807-2026 · Official record ↗
Found something wrong or missing? Report a data error.
Sources last checked October 22, 2026 at 12:00 PM UTC.