Wolf Medical recalls 6mL Luer Lock syringes with model SYR06L that may not meet safety standards due to incorrect size clearance. Affected units include specific lot codes from 2019-2022.
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Wolf Medical is recalling 6 mL Luer Lock syringes that may not meet safety standards because their size and configuration don't match the devices cleared by the manufacturer. This could lead to improper use in medical settings.
The syringes' sizes and configurations are outside the approved range for the devices the manufacturer cleared. This could mean they don't work correctly with medical devices, potentially causing errors during injections.
Healthcare professionals and patients using these syringes for medical injections may be affected. Those using the syringes for single-use procedures are most at risk.
Check for the model SYR06L on the syringe. Look for lot codes: 20191014, 20200204, 20200301, 20211112, 20220414, 20220614, or 20221015.
Look for the model number SYR06L on the syringe packaging or label.
Check the lot code on the syringe, which may be one of the listed dates: 20191014, 20200204, 20200301, 20211112, 20220414, 20220614, or 20221015.
The syringes' sizes and configurations are outside the approved range for the devices cleared by the manufacturer, which could lead to improper use in medical settings.
Lot codes 20191014, 20200204, 20200301, 20211112, 20220414, 20220614, and 20221015 are affected.
The recall does not require immediate stop use; however, you should check the model and lot code to confirm if your syringe is affected.
We’ve drafted a message you can send Wolf Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2103-2024 — Wolf Medical Wolf Medical Hello, I own a Wolf Medical that is covered by recall Z-2103-2024 from Wolf Medical. 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.
