MEDLINE SYR 10ML L/L RED syringes (model 91830) may not be safe for medical use due to incorrect device clearance. Affected units include specific lot codes from June 2023.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE SYR 10ML L/L RED syringes (model 91830) were recalled because they don't meet the required medical device standards. This could lead to improper medical use if the syringes are used without proper clearance.
The syringes have sizes and configurations that don't match the medical devices cleared by the manufacturer. This could cause improper medical use if the syringes are used without proper clearance.
Medical professionals and patients using these syringes for injections may be affected. Those with specific lot codes are most at risk.
Check for the model number 91830 on the syringe. Affected units include specific lot codes listed in the recall notice.
Look for the model number 91830 on the syringe to confirm if it's affected.
The syringes have sizes and configurations that don't match the medical devices cleared by the manufacturer.
Affected lot codes include 63721010001, 63721060001, 63721070001, and other specific codes listed in the recall notice.
The recall doesn't specify a stop-use instruction, but you should check the model and lot codes to ensure safety.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2062-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2062-2024 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.
