West Pharma Services recalls Vial2Bag DC 20mm (REF 6070112 & 6070112C) due to potential adverse events with oxytocin in pregnant women. This product is single-use only and requires a prescription.
Adverse events have been reported with the use of oxytocin in conjunction with the 13mm Vial2Bag DC in pregnant women. Vial2Bag DC 20mm is recalled due to similarities with 13mm Vial2Bag DC.
West Pharma Services is recalling Vial2Bag DC 20mm products (REF 6070112 and 6070112C) because they are similar to a 13mm version that has caused adverse events in pregnant women using oxytocin. These products are single-use only and require a prescription.
The recalled Vial2Bag DC 20mm products are similar in design to a 13mm version that has been linked to adverse events when used with oxytocin in pregnant women. This similarity could lead to incorrect usage or dosing in clinical settings.
Pregnant women using oxytocin with the recalled Vial2Bag DC 20mm products may experience adverse events. The products are single-use only and require a prescription.
Check for product references 6070112 or 6070112C on the packaging. The lot numbers listed in the recall include many specific numbers like 7689, 7690, and others. These products are single-use only and require a prescription.
Look for product references 6070112 or 6070112C on the packaging.
The Vial2Bag DC 20mm products are similar to a 13mm version that has caused adverse events when used with oxytocin in pregnant women.
The recall record does not specify a remedy, so no action is required beyond checking if you have the recalled product.
The recall indicates potential adverse events with oxytocin in pregnant women, but the product is designed for single-use only and requires a prescription.
We’ve drafted a message you can send West Pharma Services to request your refund or repair — edit it as you like.
Subject: Recall Z-0769-2019 — West Pharma Services West Pharma Services Hello, I own a West Pharma Services that is covered by recall Z-0769-2019 from West Pharma Services. 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.
