Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1831-2026 — Medline Syringes: 1) SYRINGE 12ML CONTROL W/ROTATOR, Model Number: DYNJSYR12CWR; 2) SYRINGE 10ML CONTROL W/ROTATOR, Model Number: DYNJSYR10CWR; 3) SYR CONTROL PAD 12ML L/L, Model Number: DYNJSYR12CP; 4) TBG PRESS 72IN M/F ROT BRAID, Model Number: DYNJBRT72R; 5) SYRINGE 10ML CONTROL MLL, Mod

U.S. FDA — Device Enforcement · United States · 2026-02-25 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1831-2026
Date of alert: 2026-02-25
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medline Industries, LP
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10884389676486

Reported risk: The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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