West Pharma Services recalls Vial2Bag Transfer Device (REF 6: 6070104) due to reported oxytocin risks in pregnant women using 13mm Vial2Bag DC. Affected units have specific lot numbers.
Adverse events have been reported with the use of oxytocin in conjunction with the 13mm Vial2Bag DC in pregnant women. Vial2Bag is recalled due to similarities with 13mm Vial2Bag DC.
West Pharma Services is recalling its Vial2Bag Transfer Device (REF 6070104) because adverse events have been reported with oxytocin use in pregnant women. This recall is due to similarities between this device and the 13mm Vial2Bag DC model.
Adverse events have been reported when oxytocin is used with the 13mm Vial2Bag DC in pregnant women. The recall is due to similarities between this device and the 13mm Vial2Bag DC model, which may pose risks during pregnancy.
Pregnant women using oxytocin with the Vial2Bag Transfer Device may be affected. The recall targets specific lot numbers of the device.
Check for the product name 'Vial2Bag Transfer Device' with reference number 6070104. Affected units have specific lot numbers listed in the recall notice.
Identify the reference number and lot numbers listed in the recall notice to confirm if your device is affected.
The recall is due to reported adverse events with oxytocin use in pregnant women using the 13mm Vial2Bag DC model, which this device is similar to.
Affected lot numbers include 7885, 7889, 8300, 8391, 8646, 8788, 8950, 9038, 9039, 9166, 9167, 9669, 9682, 9982, A672, and C063, C070.
The recall notice states that the remedy is null, meaning no specific action is required beyond checking if your device is affected.
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-0768-2019 — West Pharma Services West Pharma Services Hello, I own a West Pharma Services that is covered by recall Z-0768-2019 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.
