MEDLINE recalls SYR 5ML L/L GREEN syringes (model 91826) as they may not meet FDA clearance standards for size, potentially causing improper use.
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 GREEN syringes (model 91826) because their size and configuration don't match the FDA-cleared devices. This could lead to incorrect dosing or improper use if used with medical devices that require specific syringe sizes.
The syringes' sizes and configurations are outside the range of devices cleared by the manufacturer's FDA 510(k) process. This mismatch could result in incorrect dosing or improper use when interacting with medical devices that require specific syringe dimensions.
Users of these syringes for medical purposes, particularly those administering medications requiring precise syringe sizes. Healthcare providers and patients using the syringes for single-use injections are most at risk.
Check for the model number 91826 on the syringe packaging or label. These syringes are non-sterile and come without needles for single-use applications.
Look for the model number 91826 on the syringe packaging or label to confirm if it is recalled.
The recall indicates the syringes may not meet FDA clearance standards for size, so they could pose a risk of incorrect dosing or improper use with medical devices.
The recall does not specify a remedy, so check the model number 91826 to confirm if they are affected and contact the manufacturer for further guidance.
The syringes' sizes and configurations are outside the range cleared by the manufacturer's FDA 510(k), which could lead to incorrect dosing or improper use with medical devices.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2058-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2058-2024 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.
