Arrow recalls FlexTip Plus Combined Spinal Epidural Catheterization Kit ASK-05560-WH due to incorrect expiration date on lidstock. This may lead to expired product use.
Product lidstock contains the incorrect expiration date for the product
Arrow is recalling a specific spinal epidural catheterization kit because the product lidstock has the wrong expiration date. Using this kit with an incorrect expiration date could lead to expired product use.
The product lidstock contains an incorrect expiration date. This means the user might be using a kit that has expired, which could lead to ineffective or unsafe medical procedures.
Healthcare professionals who use the Arrow FlexTip Plus Combined Spinal Epidural Catheterization Kit ASK-05560-WH. Those most at risk are users who might not check the expiration date carefully.
Check for the product name 'Arrow FlexTip Plus Combined Spinal Epidural Catheterization Kit ASK-05560-WH' and lot number 13F18A0714 on the lidstock.
Verify the expiration date on the lidstock of the product. If it's incorrect, stop using the kit.
The product lidstock contains the incorrect expiration date for the product.
Check the expiration date on the lidstock. If it's incorrect, stop using the kit.
The official recall does not mention a fix; users should check the expiration date and stop using if incorrect.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1239-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1239-2020 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.
