Arrow recalls specific 18G medical kits (SAC-01218-B/C) for potential sterility problems that could cause serious infections or injuries.
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 is recalling certain 18-gauge medical kits that may have sterility issues. If the kits are contaminated, they could lead to serious infections or injuries during medical procedures.
The supplier had quality issues with the kits, which could compromise the sterility of the injectable products. If the products are not sterile, they might cause serious infections or injuries when used in medical procedures.
Healthcare professionals and patients using the recalled medical kits for injections or procedures. Those with the specific kit models and batch numbers are most at risk.
Check for kit models: SAC-01218-B, SAC-01218-C, or SAC-01618-B. Look for batch numbers starting with 10801902225303, 10801902225273, or 10801902225310.
Identify the kit model number on the product (e.g., SAC-01218-B, SAC-01218-C, SAC-01618-B).
Check the batch number on the product label, which starts with 10801902225303, 10801902225273, or 10801902225310.
The supplier had quality issues with the kits, which could compromise the sterility of the injectable products, potentially leading to serious infections or injuries.
Check the kit model and batch number to see if it matches the recalled items. If it does, contact Arrow for instructions.
If the kits are not sterile, they could cause serious infections or injuries during medical procedures.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2390-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2390-2026 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.
