MEDLINE recalls 10ml L/L blue syringes (model 91880) due to incorrect size configurations not matching cleared devices. Affected units include specific lot codes; consumers should contact MEDLINE for details.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling 10ml liquid syringes (model 91880) because their size and configuration don't match the medical devices they were cleared for. This could lead to improper use in medical settings if the syringes are used without proper compatibility.
The syringes have sizes and configurations that don't match the medical devices the manufacturer cleared for. This could cause improper use if the syringes are used without the correct compatibility, potentially leading to treatment errors.
Healthcare professionals and patients using the recalled syringes for medical treatments. Those with the specific lot codes listed are most at risk.
Check for the model number 91880 on the syringe packaging. Look for lot codes: 63720120007, 63721110003, 63721120004, 63722010001, 63722020002, 63722030002, 63722060003, 63722070002, 63723100003, 63723110005, 63723120002.
Look for the lot codes listed in the recall notice to determine if your syringes are affected.
Reach out to MEDLINE directly for specific instructions on how to handle the recalled syringes.
The recall states the syringes have sizes and configurations that don't match cleared devices, so they may not be safe for medical use without proper compatibility.
Contact MEDLINE directly for specific instructions on how to handle the recalled syringes.
Check for the model number 91880 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-2098-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2098-2024 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.
