MEDLINE recalls 10ml purple syringes (model 91842) that may not meet medical device safety standards. These non-sterile syringes could pose risks if used improperly.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling 10ml purple syringes (model 91842) that may not meet medical device safety standards. Using these syringes could lead to improper medical procedures if they don't fit the intended medical devices.
The syringes may not fit properly with medical devices cleared by the manufacturer, potentially causing improper use. This could lead to ineffective medical procedures or complications if the syringes are not designed correctly for the intended use.
Healthcare professionals and patients who use these syringes for medical procedures may be affected. Those using the syringes for non-medical purposes are less likely to be at risk.
Check for the model number 91842 on the syringe packaging. The syringes are non-sterile and come in purple with a 10ml capacity. They were sold with specific lot codes listed in the recall notice.
Look for the model number 91842 and lot codes listed in the recall notice to confirm if your syringes are affected.
The recall states that these syringes may not meet medical device safety standards, so they should not be used for medical procedures.
Check the model number and lot codes to see if your syringes are affected. If they are, contact MEDLINE for further instructions.
Yes, these are non-sterile syringes designed for single-use medical procedures.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2074-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2074-2024 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.
