MEDLINE 10ml syringes (model 91876) may not fit medical devices cleared by the manufacturer, posing risks during use. Consumers should check lot codes and contact MEDLINE for details.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE's 10ml syringes (model 91876) were recalled because their size and configuration don't match medical devices approved by the manufacturer. This could lead to improper use in medical settings.
The syringes' size and configuration are outside the range of devices cleared by the manufacturer. This means they might not work properly with medical equipment, potentially causing errors during procedures.
Healthcare professionals and patients using these syringes for medical procedures may be affected. Those using the syringes for non-medical purposes are less at risk.
Check for the model number 91876 on the syringe packaging. Look for lot codes: 63721010004, 63721040002, 63721050002, 63721080003, 63721100001, 63721100003, 63721110001, 63722010001, 63722030001, 63722050001, 63722100003, 63723030001, 63723060005, 63723070001.
Look for the model number 91876 on the syringe packaging or label.
Reach out to MEDLINE for further assistance or to confirm if your syringe is affected.
The recall indicates the syringes may not fit medical devices cleared by the manufacturer, so they are not recommended for medical use.
Lot codes 63721010004, 63721040002, 63721050002, 63721080003, 63721100001, 63721100003, 63721110001, 63722010001, 63722030001, 63722050001, 63722100003, 63723030001, 63723060005, 63723070001 are affected.
The recall does not require immediate stop use; however, healthcare professionals should avoid using these syringes for 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-2094-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2094-2024 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.
