Arrow recalls FLEXTIP Plus Epidural Catheter kits with incorrect adhesive due to supplier error. Affected units have specific UDI codes and batch numbers. Consumers should contact Arrow for details.
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Arrow is recalling FLEXTIP Plus Epidural Catheter kits and Flexblock Continuous Peripheral Nerve Block Catheter Kit/sets that were manufactured with incorrect adhesive. This issue could lead to improper function of the catheter, but the recall does not specify a risk of injury or harm to users.
The catheter kits were manufactured with incorrect adhesive due to a supplier error. This could result in improper bonding or function of the catheter, potentially affecting the procedure's effectiveness. However, the recall does not specify any risk of injury or harm to users.
Healthcare professionals who use these catheter kits for epidural anesthesia procedures are most likely affected. Patients receiving these procedures may also be impacted if the kits are used without proper adherence to the recall.
Check for the product code ASK-05502-BSM and UDI code (01)10801902209853(17)270831(11)251210(10)33F25K0409 on the packaging. The batch number is 33F25K0409.
Verify the product code ASK-05502-BSM and UDI code (01)10801902209853(17)270831(11)251210(10)33F25K0409 on the packaging.
The product was manufactured with incorrect adhesive due to a supplier error, which could affect the catheter's function.
The recall does not specify any risk of injury or harm to users.
Check for the product code ASK-05502-BSM and UDI code (01)10801902209853(17)270831(11)251210(10)33F25K0409 on the packaging.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1913-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1913-2026 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.
