B. Braun Medical, Inc.: Medical Device Recall in 2014 - (Recall #: Z-2655-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

B.Braun Accuflo 100ML/H 100ML Elastomeric Infusion Device. AccuFlo devices are intended for patients requiring intravenous, percutaneous, subcutaneous, intra-operative sites or epidural administration of medications.

Product Classification:

Class II

Date Initiated: August 6, 2014

Date Posted: September 24, 2014

Recall Number: Z-2655-2014

Event ID: 69054

Reason for Recall:

The primary packaging label (inner pouch label) indicates that the package contents are Catalog Item: CT-1000-250, while the secondary packaging label (outer carton label) indicates the contents are CT-1000-100. The actual contents are a CT-1000-100.

Status: Terminated

Product Quantity: 8,640 units

Code Information:

Lot Number: 4A1125F111

Distribution Pattern:

Distributed in the state of Missouri.

Voluntary or Mandated:

Voluntary: Firm initiated