MEDLINE recalls SYR 10ML L/L YELLOW LIDO syringes (model 91854) due to piston size mismatch with cleared devices. These non-sterile syringes without needles may not be safe for intended use.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling SYR 10ML L/L YELLOW LIDO syringes (model 91854) because their piston size doesn't match the medical devices they were cleared for. This could mean the syringes aren't safe for use as intended.
The syringes have piston sizes that don't match the medical devices cleared by the manufacturer. This mismatch could mean the syringes aren't safe for the intended medical procedures, potentially causing injury or improper treatment.
People who own or use MEDLINE SYR 10ML L/L YELLOW LIDO syringes (model 91854) with lot codes 63721060001, 63721110001, 63722120002, or 63723070001 are affected. Healthcare workers using these syringes for medical procedures are at higher risk.
Check for the model number 91854 on the syringe packaging. Look for lot codes 63721060001, 63721110001, 63722120002, or 63723070001 on the syringe or packaging.
Verify the model number is 91854 and lot code matches one of the listed codes.
The recall states the syringes have piston sizes outside the cleared range, so they may not be safe for intended medical use. MEDLINE recommends not using them.
The recall does not specify a remedy, so you should check with MEDLINE directly for guidance.
Look for model number 91854 and lot codes 63721060001, 63721110001, 63722120002, or 63723070001 on the syringe or packaging.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2082-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2082-2024 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.
