MEDLINE SYR 60ML L/S non-sterile syringes with model 83079 are recalled because they don't meet cleared device standards. This could lead to improper use in medical settings.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE SYR 60ML L/S non-sterile syringes (model 83079) are being recalled because their piston sizes and configurations don't match the medical devices cleared by the manufacturer. This could cause improper use in medical procedures if used without proper compatibility.
The syringes have piston sizes and configurations that don't match the medical devices cleared by the manufacturer. This could lead to improper use during medical procedures if the syringes are not compatible with the intended medical devices.
Healthcare professionals and medical facilities that use these syringes are likely affected. The risk is low as the issue relates to device clearance rather than immediate safety hazards.
Check for the model number 83079 on the syringe packaging or label. The lot codes listed (e.g., 63721010004, 63721020002) indicate specific batches that are affected.
Look for the model number 83079 and lot codes such as 63721010004 or 63721020002 on the syringe packaging.
The recall indicates the syringes may not meet cleared device standards, so they should not be used for medical procedures without verification.
Check the model number and lot codes on the syringe packaging to see if they are affected. If so, stop using them and contact MEDLINE for further instructions.
Look for the model number 83079 and lot codes listed in the recall (e.g., 63721010004, 63721020002) on the syringe packaging.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2044-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2044-2024 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.
