WEST PHARMA. SERVICES IL, LTD: Vial2BAG Transfer Device, REF 6070104, Single use only, Rx Only

Is my product affected?

Vial2BAG Transfer Device, REF 6070104, Single use only, Rx Only

• UPC 07290108240047

Check against the official notice below — it lists the full affected range.

What happened

West Pharma. Services IL, Ltd. is recalling the Vial2BAG Transfer Device (REF 6070104), a single-use prescription medical device. The recall was initiated because adverse events have been reported when oxytocin was used with a similar product called the 13mm Vial2Bag DC in pregnant women. Due to similarities between the products, the Vial2BAG Transfer Device is being recalled as a precaution. Approximately 4.9 million units were distributed in the United States through a distributor in Missouri.

The affected products include specific lot numbers: 7885, 7889, 8300, 8391, 8646, 8788, 8950, 9038, 9039, 9166, 9167, 9669, 9682, 9982, A672, C063, and C070. The source document does not specify what actions affected consumers should take in response to this recall.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: US Distributor in MO Quantity: 4.9 million units Lot/code info: UDI: (01)07290108240047(17)190301(10)7885(90)36098093(91)6070104 Lot Numbers: 7885, 7889, 7889, 8300, 8391, 8646, 8788, 8950, 9038, 9039, 9166, 9167, 9669, 9682, 9982, A672, C063, C070

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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