Labories Medical Technologies recalls injeTAK Adjustable Tip Needles with damaged packaging that may compromise sterile barrier. Affected models include DIS199 and DIS201 with specific lot numbers. Consumers should stop using and contact for replacement.
The packaging may be damaged, compromising the sterile barrier.
Labories Medical Technologies is recalling injeTAK Adjustable Tip Needles due to packaging that may be damaged, risking contamination. This could lead to infections if the needles are used without a sterile barrier.
The packaging may be damaged, compromising the sterile barrier that protects the needles from contamination. If the packaging is compromised, the needles could become contaminated during use, leading to infections.
Medical professionals and patients using the injeTAK needles for injections. Those who have the specific model numbers and lot codes listed are most at risk.
Check for model numbers DIS199 or DIS201 with the specific lot codes listed in the recall notice. The needles have a diameter of 6Fr and length of 35-50cm.
Immediately stop using the recalled injeTAK needles if you have the affected model numbers and lot codes.
Reach out to Labories Medical Technologies for a replacement or refund using the provided lot numbers.
The recalled models are DIS199 and DIS201 with specific lot numbers listed in the recall notice.
Check the model number and lot code on the packaging. Affected models include DIS199 and DIS201 with the specific lot numbers listed in the recall notice.
The recall does not state that the needles need to be discarded; instead, contact Labories Medical Technologies for a replacement or refund.
We’ve drafted a message you can send Labories Medical Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1478-2023 — Labories Medical Technologies Labories Medical Technologies Hello, I own a Labories Medical Technologies that is covered by recall Z-1478-2023 from Labories Medical Technologies. 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.
