WEST PHARMA. SERVICES IL, LTD: Medical Device Recall in 2019 - (Recall #: Z-0768-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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

Product Classification:

Class I

Date Initiated: December 26, 2018

Date Posted: February 6, 2019

Recall Number: Z-0768-2019

Event ID: 81877

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.

Status: Terminated

Product Quantity: 4.9 million units

Code Information:

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

Distribution Pattern:

US Distributor in MO

Voluntary or Mandated:

Voluntary: Firm initiated