MEDLINE recalls 10ml L/L red LIDO syringes (model 91850) due to incorrect device clearance. These non-sterile syringes without needles may not be safe for medical use. Consumers should contact MEDLINE for details.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling 10ml L/L red LIDO syringes (model 91850) because they were not cleared for use as intended. This could lead to unsafe medical procedures if used without proper device compatibility.
The syringes were manufactured with sizes and configurations that do not match the medical devices cleared by the manufacturer. This means they may not function safely during medical procedures, potentially causing injury or ineffective treatment.
Medical professionals and patients who own or use these specific syringes are affected. Those using the syringes for medical procedures are at higher risk.
Check for the model number 91850 on the syringe packaging. The syringes are non-sterile and come without needles for single use. Look for lot codes: 63721040002, 63721120001, 63722010001, 63722080002, 63722100003, 63723100003, 63723110001.
Look for the model number 91850 and lot codes listed above on the syringe packaging.
The syringes were manufactured with sizes and configurations that do not match the medical devices cleared by the manufacturer, which could lead to unsafe use.
Check for the model number 91850 and lot codes: 63721040002, 63721120001, 63722010001, 63722080002, 63722100003, 63723100003, 63723110001 on the syringe packaging.
The recall record does not specify a remedy, so contact MEDLINE directly for instructions.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2079-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2079-2024 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.
