Medline recalls 0.9% Sodium Chloride Injection in 10mL syringes due to incorrect overwrap packaging. This may lead to improper use during IV procedures. Affected lots: 3131591.
Packaged with an incorrect overwrap.
Medline is recalling 0.9% Sodium Chloride Injection in 10mL syringes because they were packaged with the wrong overwrap. This could cause improper use during IV procedures if the syringe is not handled correctly.
The incorrect overwrap packaging may not properly seal the syringe, potentially allowing contamination or improper handling during IV procedures. This could lead to incorrect medication administration if the syringe is not used as intended.
Healthcare professionals using IV equipment who may have received this specific lot number (3131591). Patients receiving IV treatments with this syringe could be at risk if the overwrap issue leads to improper handling.
Check for the lot number 3131591 on the syringe packaging. The product is a 0.9% Sodium Chloride Injection in 10mL syringes intended for IV catheter flushing.
Look for the lot number 3131591 on the syringe packaging to confirm if it is affected.
The recall is due to incorrect overwrap packaging, which may lead to improper handling during IV procedures. If you have the lot number 3131591, you should check the packaging and follow the action steps.
Check the lot number on the syringe packaging. If it is 3131591, you should stop using it and contact Medline for further instructions.
The hazard is related to incorrect overwrap packaging, which could lead to improper handling during IV procedures. However, the risk is low and does not involve immediate danger to users.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2948-2018 — Medline Medline Hello, I own a Medline that is covered by recall Z-2948-2018 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.
