MEDLINE recalls SYR 10ML L/L GREEN CONT syringes (model 91857) due to incorrect size configuration for medical devices. This may cause improper use in medical procedures.
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 green syringes (model 91857) because they don't match the medical device clearance standards. Using these syringes could lead to improper medical procedures if they're not the correct size for the intended use.
The syringes have sizes and configurations that don't match the medical devices cleared by the manufacturer. This could lead to improper use during medical procedures, potentially causing incorrect dosing or ineffective treatment.
Healthcare professionals and medical facilities that use these syringes for procedures. Patients receiving injections with these syringes may be at risk of incorrect dosing.
Look for syringes labeled 'MEDLINE SYR 10ML L/L GREEN CONT' with model number 91857. These are non-sterile syringes without needles for single use.
Verify the model number on the syringe is 91857 and the product name is SYR 10ML L/L GREEN CONT.
The recall states these syringes have sizes and configurations outside the cleared device range, so they may not be safe for intended medical use.
The recall does not specify a remedy, so you should check with MEDLINE for guidance if you have these syringes.
Look for syringes labeled 'MEDLINE SYR 10ML L/L GREEN CONT' with model number 91857.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2085-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2085-2024 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.
