2,784 recent recalls from the U.S. Food & Drug Administration in our current data (last 90 days). Showing 2,701–2,784, newest first.
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1891-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1890-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1889-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1888-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1887-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1886-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1885-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1884-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1883-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1882-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1881-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1880-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1879-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1878-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1877-2026 · Official record ↗
Unapproved design changes to the products outside of the 510(k) clearance.
Company / brand: Medline Industries recalls
Official ID Z-1876-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1875-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1874-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1873-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1872-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1871-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1870-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1869-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1868-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1867-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1866-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1865-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1864-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1863-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1862-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1861-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1860-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1859-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1858-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1857-2026 · Official record ↗
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Company / brand: Angiodynamics recalls
Official ID Z-1856-2026 · Official record ↗
Potential for detachment of a distal tip component of the device during use.
Company / brand: Olympus of the Americas recalls
Official ID Z-1854-2026 · Official record ↗
Potential for detachment of a distal tip component of the device during use.
Company / brand: Olympus of the Americas recalls
Official ID Z-1853-2026 · Official record ↗
Potential for detachment of a distal tip component of the device during use.
Company / brand: Olympus of the Americas recalls
Official ID Z-1852-2026 · Official record ↗
Potential for detachment of a distal tip component of the device during use.
Company / brand: Olympus of the Americas recalls
Official ID Z-1851-2026 · 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
Official ID Z-1850-2026 · 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
Official ID Z-1849-2026 · 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
Official ID Z-1848-2026 · 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
Official ID Z-1847-2026 · 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
Official ID Z-1846-2026 · 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
Official ID Z-1845-2026 · 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
Official ID Z-1844-2026 · 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
Official ID Z-1843-2026 · 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
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
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
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
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
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
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
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
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
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
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
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
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
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
Official ID Z-1829-2026 · Official record ↗
Software issue that renders the touch screen unresponsive.
Company / brand: Integra LifeSciences (NeuroSciences) recalls
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
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
Official ID Z-1807-2026 · Official record ↗
Undeclared hazelnut and soy lecithin.
Company / brand: Costco Wholesale recalls
Official ID H-0682-2026 · Official record ↗
Undeclared milk.
Company / brand: Marquez Brothers International recalls
Official ID H-0674-2026 · Official record ↗
Undeclared milk.
Company / brand: Marquez Brothers International recalls
Official ID H-0673-2026 · Official record ↗
Undeclared milk.
Company / brand: Marquez Brothers International recalls
Official ID H-0672-2026 · Official record ↗
Lead level was higher than NYSAGM Standard.
Company / brand: Summit Import recalls
Official ID H-0671-2026 · Official record ↗
Product(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40
Company / brand: Ethnic Foods recalls
Official ID H-0670-2026 · Official record ↗
Product(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40
Company / brand: Ethnic Foods recalls
Official ID H-0669-2026 · Official record ↗
Hard corn starch lumps were found in the product
Company / brand: Mondelez Global recalls
Official ID H-0667-2026 · Official record ↗
Product may be contaminated with Salmonella.
Company / brand: Unistel Industries recalls
Official ID H-0666-2026 · Official record ↗
Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin
Company / brand: Teva Pharmaceuticals USA recalls
Official ID D-0521-2026 · Official record ↗
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Company / brand: B BRAUN MEDICAL recalls
Official ID D-0498-2026 · Official record ↗
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Company / brand: B BRAUN MEDICAL recalls
Official ID D-0497-2026 · Official record ↗
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Company / brand: B BRAUN MEDICAL recalls
Official ID D-0496-2026 · Official record ↗
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Company / brand: B BRAUN MEDICAL recalls
Official ID D-0495-2026 · Official record ↗
Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.
Company / brand: The Harvard Drug Group recalls
Official ID D-0493-2026 · Official record ↗
Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to n…
Company / brand: Premier Dental Products Co recalls
Official ID D-0490-2026 · Official record ↗
Lack of Assurance of Sterility
Company / brand: Harrow Eye recalls
Official ID D-0489-2026 · Official record ↗
CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.
Company / brand: Leading Pharma recalls
Official ID D-0486-2026 · Official record ↗
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."
Company / brand: Hetero Labs (Unit V) recalls
Official ID D-0484-2026 · Official record ↗
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FDA last checked October 22, 2026 at 12:00 PM UTC.