Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Vial2BAG Transfer Device Recalled by WEST PHARMA. SERVICES IL, LTD Due to Adverse events have been reported with the use...

Date: December 26, 2018
Company: WEST PHARMA. SERVICES IL, LTD
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact WEST PHARMA. SERVICES IL, LTD directly.

Affected Products

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

Quantity: 4.9 million units

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed to 1 state: MO

Affected (1 state)Not affected

About WEST PHARMA. SERVICES IL, LTD

WEST PHARMA. SERVICES IL, LTD has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report