MEDLINE recalls 10ml L/L red syringes (model 91878) that may not meet medical device safety standards. These non-sterile syringes could pose risks if used without proper clearance.
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 syringes (model 91878) because they may not meet medical device safety standards. Using these syringes could lead to improper medical procedures if they don't match the intended device clearance.
The syringes may not meet the required medical device safety standards due to incorrect sizes and configurations. This could lead to improper medical procedures if used without proper clearance.
Healthcare professionals and patients using these syringes for medical procedures. Those with the specific lot codes listed are most at risk.
Check for the model number 91878 on the syringe packaging. Look for lot codes: 63721070004, 63722010001, 63722030001, 63722050001, 63722080002, 63722080004, 63722120004, 63723030001, 63723050001, 63723060005, 63723120002.
Look for the specific lot codes listed in the recall notice to identify affected units.
The recall indicates these syringes may not meet medical device safety standards, so they should not be used without confirming they are cleared for your intended purpose.
Check the lot code on the syringe packaging to see if it matches the listed codes. If it does, stop using them and contact MEDLINE for further instructions.
Look for the model number 91878 and the specific lot codes listed in the recall notice.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2096-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2096-2024 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.
