West Pharmaceutical Services recalls Vial2Bag Advanced 20mm Admixture Devices due to heat exposure causing packaging damage that may breach sterile barriers. Affected units include specific model and lot numbers.
Due to packaging damage from heat exposure during shipping/transportation that may result in a breach in the sterile barrier.
West Pharmaceutical Services is recalling Vial2Bag Advanced 20mm Admixture Devices because heat exposure during shipping might damage the packaging, potentially breaching the sterile barrier. This could lead to contamination of the device and unsafe use of medications.
The device's packaging may be damaged by heat during shipping, which could cause a breach in the sterile barrier. This might allow contaminants to enter the device, potentially leading to medication contamination.
Healthcare professionals and patients using the Vial2Bag Advanced 20mm Admixture Device for medication reconstitution are affected. Those using the specific model and lot numbers listed in the recall are most at risk.
Check for the model number 6070030 and lot numbers K188 or K194 on the device packaging. The product is sold as a single-use device for reconstituting medications.
Look for the model number 6070030 and lot numbers K188 or K194 on the device packaging.
The recalled model number is 6070030.
Lot numbers K188 and K194 are affected.
The recall record does not specify a remedy.
We’ve drafted a message you can send Vial2Bag Advanced to request your refund or repair — edit it as you like.
Subject: Recall Z-0283-2025 — Vial2Bag Advanced Vial2Bag Advanced Hello, I own a Vial2Bag Advanced that is covered by recall Z-0283-2025 from Vial2Bag Advanced. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.