Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes: recall status ⚠ Recalls found. Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes is named in 16 official recalls in our current data:
FDA Class II recall Z-2581-2026 — Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.FDA Class II recall Z-2582-2026 — Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.FDA Class II recall Z-2583-2026 — Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.And 13 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 · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2581-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2582-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2583-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2584-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2585-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2586-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2587-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2588-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2589-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2590-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2591-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2592-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2593-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2594-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2595-2026 ·
Official record ↗
FDA Class II · Medical device · July 1, 2026
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
Company / brand: Medline Industries
Affected product: Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes
Official ID Z-2596-2026 ·
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.