MEDLINE recalls 10ml L/S white Lido syringes (model 91873) due to incorrect device clearance. These non-sterile syringes without needles may not meet safety standards 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 10ml L/S white Lido syringes (model 91873) because they were cleared for use without meeting the required safety standards. This could lead to improper medical procedures if used incorrectly.
The syringes were cleared for use without meeting the required safety standards. This means they may not function correctly during medical procedures, potentially causing harm.
Healthcare professionals and patients using these syringes for medical procedures are affected. Those using the syringes for injections or other medical treatments are at risk.
Check for the model number 91873 on the syringe packaging. These non-sterile syringes without needles are sold by MEDLINE for single-use medical procedures.
Look for the model number 91873 on the syringe packaging to confirm if it is recalled.
The syringes were cleared for use without meeting the required safety standards, which could lead to improper medical procedures.
The official recall record states that these syringes may not meet safety standards, so they should not be used.
Check for the model number 91873 on the syringe packaging. These non-sterile syringes without needles are sold by MEDLINE for single-use medical procedures.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2092-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2092-2024 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.
