MEDLINE SYR 10ML L/L GREEN syringes (model 91831) may not be safe for medical use due to incorrect device configurations. Affected units include specific lot codes from June 2023. Consumers should contact MEDLINE for details.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
MEDLINE SYR 10ML L/L GREEN syringes (model 91831) are being recalled because they don't match the medical device standards approved by the FDA. This could lead to unsafe medical procedures if used without proper compatibility.
The syringes have sizes and configurations that don't match the medical devices cleared by the manufacturer's FDA approval. This means they might not work safely with certain medical equipment, potentially causing errors during procedures.
People who own or use these syringes for medical purposes, especially those who have the specific lot codes listed in the recall notice.
Check for the model number 91831 and lot codes listed: 63720120007, 63721010001, 63721070001, 63721080001, 63721090001, 63721100001, 63721110001, 63721120001, 63722020002, 63722030001, 63722040002, 63722050001, 63722060001, 63722070002, 63722080002, 63722090002, 63722120002, 63723020001, 63723030001, 63723050001, 63723060001, 63723070001, 63723090002, 63723100003, 63723120002.
Look for the model number 91831 and the specific lot codes listed in the recall notice.
The syringes have sizes and configurations that don't match the medical devices cleared by the manufacturer's FDA approval, which could lead to unsafe medical procedures.
Contact MEDLINE directly to get details about the specific lot codes and any necessary actions.
The recall indicates potential incompatibility with medical devices, but no specific injuries have been reported. Using them could lead to errors during medical procedures.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2063-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2063-2024 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.
