MEDLINE recalls SYR 3ML L/L BLUE syringes (model 91822) as they may not meet FDA clearance standards for their size, posing potential safety risks.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling SYR 3ML L: L BLUE syringes (model 91822) because they may not meet FDA clearance standards for their size. This could lead to improper medical use if the syringes are used without proper compatibility.
The syringes may not meet the FDA's clearance standards for their size, which could lead to improper medical use if the syringes are not compatible with the intended medical devices. This might result in ineffective treatment or injury.
Users of MEDLINE SYR 3ML L/L BLUE syringes (model 91822) who are medical professionals or patients requiring single-use syringes. Those using these syringes for medical procedures are most at risk.
Check for the model number 91822 on the syringe packaging or label. These syringes are non-sterile and intended for single use without needles.
Verify the model number on the syringe packaging or label to confirm it is 91822.
The syringes may not meet FDA clearance standards for their size, which could lead to improper medical use.
The recall indicates they may not meet FDA clearance standards, so they should not be used without confirming the model number.
Check the model number on the packaging or label to confirm if it is 91822. If so, contact MEDLINE for further instructions.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2056-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2056-2024 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.