Arrow recalls Large Volume Abdominal Paracentesis Kit AK 00376 due to potential packaging not being completely sealed. This could lead to contamination risks during medical procedures.
Product packaging may not be completely sealed.
Arrow is recalling its Large Volume Abdominal Paracentesis Kit (AK : 00376) because the packaging might not be sealed properly. This could cause contamination during medical procedures if the kit is used without the packaging being fully secure.
The packaging may not be completely sealed, which could allow contaminants to enter the kit during use. This poses a risk of infection or contamination during medical procedures if the kit is not properly protected.
Healthcare professionals who use this medical kit for abdominal fluid drainage procedures are likely affected. Patients undergoing such procedures with this kit could be at risk if the packaging isn't sealed properly.
Check for the product name 'Large Volume Abdominal Paracentesis Kit' and model number AK 00376. This kit was sold by Arrow International Inc.
Inspect the packaging for any signs of incomplete sealing.
The recall is due to potential packaging not being completely sealed, which could lead to contamination risks during medical procedures. However, the risk is low and the kit may still be safe if the packaging is properly sealed.
Look for the product name 'Large Volume Abdominal Paracentesis Kit' and model number AK 00376. This kit was sold by Arrow International Inc.
The recall does not specify a remedy, so check the packaging seal for completeness. If the seal is incomplete, contact Arrow International Inc. for further guidance.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1297-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1297-2018 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.
