Medline recalls sterile double swivel suction catheters that were distributed before sterilization. This could lead to infection if used without proper sterilization. Affected products have specific model and lot numbers.
Products labeled as sterile were distributed prior to sterilization
Medline is recalling double swivel suction catheters that were distributed before being sterilized. Using these unsterilized products could lead to infection if they come into contact with open wounds or bodily fluids.
The catheters were distributed without proper sterilization, meaning they could be contaminated. If used without sterilization, they might introduce infections into the body, especially during medical procedures involving open wounds or bodily fluids.
Healthcare professionals and patients using these catheters for endotracheal tube procedures. Those most at risk are individuals who have used the unsterilized products for medical procedures.
Check for the model number DYNCSDS12 and lot number 28617070015 on the product packaging. These catheters are labeled as sterile and are 21.3 inches long for endotracheal tube use.
Look for the model number DYNCSDS12 and lot number 28617070015 on the product packaging.
The products were distributed before sterilization, which could lead to contamination and infection if used without proper sterilization.
The recall record does not specify a remedy, so there is no action required beyond checking if you have the affected product.
No, the unsterilized products could lead to infection if used without proper sterilization.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0113-2018 — Medline Medline Hello, I own a Medline that is covered by recall Z-0113-2018 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.
