MEDLINE recalls SYR 10ML L/L BLUE LIDO syringes (model 91847) because they don't match the cleared device sizes. These non-sterile syringes without needles may not be safe for medical use.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling SYR 10ML L/L BLUE LIDO syringes (model 91847) because they have sizes and configurations that don't match the medical devices cleared by the manufacturer. This could mean the syringes aren't safe for use in medical procedures.
The syringes have sizes and configurations that don't match the medical devices cleared by the manufacturer. This could mean they aren't safe for medical use, potentially causing incorrect dosing or injury.
Medical professionals and patients who own or use these non-sterile syringes without needles may be affected. Those using the syringes for medical procedures are at higher risk.
Check for the model number 91847 on the syringe packaging. Look for lot codes: 63721010001, 63721100001, 63722050001, 63722060001, 63722070002, 63723010001.
Look for the model number 91847 and lot codes listed above on the syringe packaging.
The recall states the syringes have sizes and configurations that don't match cleared devices, so they may not be safe for medical use.
The recall doesn't specify a remedy, so you should check with the manufacturer or healthcare provider for guidance.
Check for the model number 91847 and lot codes: 63721010001, 63721100001, 63722050001, 63722060001, 63722070002, 63723010001.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2077-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2077-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.