Arrow recalls Blue PSI Kit Cath-Gard for possible incorrect banner card in kit. This may affect catheter use safety. Contact Arrow for details.
Products may contain the incorrect banner card within the kit
Arrow is recalling Blue PSI Kit Cath-Gard for possible incorrect banner card in the kit. This could affect catheter safety during medical procedures.
The kit may contain an incorrect banner card, which could lead to improper catheter use. This might affect the safety of the medical procedure.
Healthcare professionals using the kit with 7.5-8 Fr catheters are most at risk. Patients receiving this catheter care may be affected.
Look for the product code CDC-29803-1A on the kit. The kit is for use with 7.5-8 Fr catheters and has lot number 13F18H0610.
Verify the product code CDC-29803-1A on the kit to confirm if it is recalled.
The recall states the kit may contain an incorrect banner card, but the hazard is not described as causing serious injury.
The recall does not specify a remedy, so contact Arrow directly for guidance.
Look for product code CDC-29803-1A and lot number 13F18H0610 on the kit.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2555-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2555-2019 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.
