Medline recalls specific Namic Syringes due to rescinded 510(k) regulatory clearances. Affected models include DYNJSYR10CWRB with certain lot numbers. Consumers should check their syringes for these identifiers.
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline is recalling specific Namic Syringes that have rescinded 510(k) regulatory clearances. This means the syringes may not meet safety standards for medical use, potentially causing harm during procedures.
The 510(k) regulatory clearances for these syringes have been rescinded by the FDA, meaning they no longer meet safety standards for medical use. This could lead to improper function or injury during medical procedures.
Healthcare professionals and medical facilities using the recalled syringes are most at risk. Patients using these syringes for medical procedures could face safety issues.
Check for the model number DYNJSYR10CWRB on the syringe. Look for specific lot numbers: 25GBK394, 25GBN659, 25GBO446, 25GBO586, or 25GBQ523.
Look for the model number DYNJSYR10CWRB on the syringe.
Check if the lot number matches the affected numbers: 25GBK394, 25GBN659, 25GBO446, 25GBO586, or 25GBQ523.
The 510(k) regulatory clearances for these syringes have been rescinded by the FDA, meaning they no longer meet safety standards for medical use.
Check the model number and lot number to see if they are affected. If they match the recalled identifiers, stop using them and contact Medline for further instructions.
The rescinded 510(k) clearances indicate potential safety issues, but the exact risk is not specified in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1830-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1830-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
