⚠ Recall found. Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes is named in 16 official recalls in our current data. Details and the official notices are below — act on the remedy in the official notice.
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2581-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2582-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2583-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2584-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2585-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2586-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2587-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2588-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2589-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2590-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2591-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2592-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2593-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2594-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2595-2026 · Official record ↗
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Official ID Z-2596-2026 · Official record ↗
See all Medline Industries recalls →
Found something wrong or missing? Report a data error.
Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 1:09 AM UTC.