MEDLINE recalls SYR 5ML L/L YELLOW syringes (model 91829) because their piston sizes don't match cleared devices. This could lead to improper use in medical settings. Affected units include specific lot codes.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling SYR 5ML L/L YELLOW syringes (model 91829) because their piston sizes don't match the medical devices they were cleared for. This could cause improper use in medical settings, potentially leading to incorrect dosing or injury.
The syringes have piston sizes and configurations that don't match the medical devices cleared by the manufacturer. This could lead to improper use during injections, such as incorrect dosing or injury if used with devices not designed for them.
Healthcare professionals and patients using these syringes for medical injections. Those with specific lot codes (63721090001, 63722090002, 63722100003) are most at risk.
Check for the model number 91829 on the syringe packaging. Look for the lot codes 63721090001, 63722090002, or 63722100003 on the syringe or its packaging.
Verify the model number on the syringe is 91829 and the lot code matches one of the listed codes (63721090001, 63722090002, 63722100003).
The syringes have piston sizes and configurations that don't match the medical devices cleared by the manufacturer, which could lead to improper use during injections.
Check the model number and lot code. If it matches the recalled model and lot codes, stop using them and contact MEDLINE for guidance.
The hazard could lead to incorrect dosing or injury if used with devices not designed for them, but the recall is for medical use only.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2061-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2061-2024 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.
