MEDLINE recalls 20ml purple syringes (model 91843) that may not meet safety standards for medical use. This could lead to improper dosing if used with devices cleared under the firm's 510(k).
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling 20ml purple syringes (model 91843) because their size and configuration don't match the medical devices they were cleared for. This could cause incorrect dosing if used with devices that require specific syringe sizes.
The syringes' size and configuration don't match the medical devices they were cleared for. This could lead to incorrect dosing if used with devices that require specific syringe sizes.
Healthcare professionals and patients who use these syringes for medical injections may be affected. Those using the syringes with devices cleared under the manufacturer's 510(k) are at higher risk.
Look for MEDLINE syringes labeled 'SYR 20ML/L PURPLE' with model number 91843. These are non-sterile syringes without needles for single use.
Verify the model number on the syringe is 91843 and it's labeled as SYR 20ML/L PURPLE.
The recall states the syringes may not meet safety standards for medical use, so they should not be used with devices cleared under the manufacturer's 510(k).
The recall does not specify a remedy, so you should check with the manufacturer or healthcare provider for guidance.
The recall indicates a risk of incorrect dosing if used with devices that require specific syringe sizes, but no specific injury mechanism is described.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2128-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2128-2024 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.
