MEDLINE recalls SYR 5ML L/S non-sterile syringes (model 83085) because their piston sizes don't match cleared devices. This could cause improper use in medical settings.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling non-sterile 5ml syringes (model 83085) because their piston sizes don't match the medical devices they were cleared for. This could lead to improper use in medical procedures if the syringes are used without proper compatibility.
The syringes' piston sizes and configurations are outside the range of devices cleared by the manufacturer. This could cause improper use in medical settings if the syringes are used without proper compatibility with medical devices.
Healthcare professionals and patients using these syringes for medical procedures. Those with specific medical device compatibility requirements are most at risk.
Check for the model number 83085 on the syringe packaging. Look for lot codes: 63721010004, 63721100001, 63721110001, 63721120001, 63722010001, 63722020002, 63722030001, 63722040001, 63722050005, 63722070005, 63722080002, 63722090002, 63723070001, 63723090002, 63723100008, 63723110001, 63723120002.
Look for model number 83085 on the syringe packaging or label.
The recall states the syringes' piston sizes are out of the range of cleared devices, so they may not be safe for medical use without proper compatibility.
The recall does not specify a remedy, so you should check with your healthcare provider or the manufacturer for guidance.
Check for model number 83085 and 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-2050-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2050-2024 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.
