Baxter Healthcare Corp.: Medical Device Recall in 2013 - (Recall #: Z-0392-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Baxter, VIAL-MATE Adaptor, 2B8071, Rx Only, STERILE R, Baxter Healthcare Corporation, Deerfield, IL 30015 USA The VIAL-MATE is reconstitution device labeled for use with 20 mm drug vials and 50mL, 100mL, and 250mL Single Pack Mini Bags.

Product Classification:

Class II

Date Initiated: September 25, 2013

Date Posted: December 4, 2013

Recall Number: Z-0392-2014

Event ID: 66389

Reason for Recall:

Incomplete foil seal on one lot of sterile product.

Status: Terminated

Product Quantity: 38,400 units

Code Information:

Lot Number GR13G23028

Distribution Pattern:

Nationwide Distribution including WV, KY, IA, AR, OH, IL, IN, MI, KS, TN, WI, MN, MO.

Voluntary or Mandated:

Voluntary: Firm initiated