Arrow International LLC recalls medical kits with lidocaine, bupivacaine, and saline due to potential sterility issues. If contaminated, these products could cause serious or life-threatening injuries. Consumers should check product codes and contact Arrow for details.
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Arrow International LLC is recalling medical kits that contain lidocaine, bupivacaine, and saline. The supplier had quality issues, and if the products are contaminated, they could cause serious or life-threatening injuries. Consumers should stop using these kits and contact Arrow for instructions.
The supplier had quality issues that could compromise the sterility of the water-based injectable products. If the products are not sterile, they could cause serious or life-threatening infections or reactions when injected.
Medical professionals and patients using the recalled kits for injections or procedures. Those who have used the kits recently are at highest risk.
Check for product codes like GU-04020, AK-09803-CDC, AK-09903-CDC, or ASK-09903-UPA. These kits were sold in the U.S. and Canada between 2020 and 2023.
Immediately stop using any recalled medical kits that contain lidocaine, bupivacaine, or saline.
Reach out to Arrow International LLC for specific steps to return or replace the kits.
Arrow International LLC is recalling medical kits that contain lidocaine, bupivacaine, and saline due to potential sterility issues from the supplier. This could lead to serious or life-threatening injuries if the products are contaminated.
Check the product codes on the kit, such as GU-04020, AK-09803-CDC, AK-09903-CDC, or ASK-09903-UPA. These kits were sold in the U.S. and Canada between 2020 and 2023.
Immediately stop using the kit and contact Arrow International LLC for instructions on returning or replacing it.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2385-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2385-2026 from Arrow. 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.
