MEDLINE SYR 20ML L/L YELLOW syringes (model 91839) may not be safe for medical use due to incorrect size configurations. Recalled 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 20ML L/L YELLOW syringes (model 91839) were recalled because their size and configuration don't match medical devices cleared by the manufacturer. This could lead to improper medical use if the syringes are used without proper compatibility.
The syringes have sizes and configurations that don't match the medical devices cleared by the manufacturer. This mismatch could cause improper use during medical procedures, potentially leading to incorrect dosing or ineffective treatment.
Healthcare professionals and patients using these syringes for medical procedures may be affected. Those using the recalled model for single-use injections are at risk of improper medical application.
Check for the model number 91839 on the syringe packaging. The product is a non-sterile syringe without needles for single use. Recalled units include specific lot codes listed in the recall notice.
Identify the model number and lot codes on the syringe packaging to confirm if it's recalled.
No, these syringes have sizes and configurations that don't match medical devices cleared by the manufacturer, so they may not be safe for medical use.
Recalled lot codes include 63721040002, 63721050002, 63721070001, 63721080001, 63721090001, 63721100001, 63721110001, 63722030001, 63722050001, 63722080002, 63722100003, 63722120002, 63723020001, 63723030001, 63723050001, 63723060001, 63723070001, 63723090002, 63723100003, 63723110001.
The recall notice does not specify a replacement process or remedy.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-2071-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-2071-2024 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.
