MEDLINE SYR 20ML L/L non-sterile syringes with model 83088 may not meet FDA device clearance standards. Consumers should check lot codes listed to determine if affected.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE is recalling non-sterile 20ml syringes (model 83088) because they don't match the device clearance standards the company approved. This could mean the syringes aren't safe for medical use as intended.
The syringes have sizes and configurations that don't match the medical devices cleared by the manufacturer's FDA approval. This could lead to improper use or ineffective medical procedures if the syringes are used without proper clearance.
Medical professionals and patients who own or use these specific syringes are affected. Those using the syringes for medical procedures are at the highest risk.
Check for the model number 83088 on the syringe packaging. Look for lot codes listed: 63720120007, 63721010002, 63721010003, and other specific numbers provided in the recall notice.
Look for the lot codes listed in the recall: 63720120007, 63721010002, 63721010003, and other specific numbers provided in the recall notice.
The recall states these syringes may not meet the device clearance standards the manufacturer approved. They are not safe for medical use as intended.
Check the lot code on your syringe. If it matches the listed codes, stop using it and contact MEDLINE for further instructions.
Look for the model number 83088 and check the lot codes listed in the recall notice: 63720120007, 63721010002, 63721010003, and other specific numbers provided.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2052-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2052-2024 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.
