B. Braun Medical, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0327-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Affected Pain Control Tray Component (5% Lidocaine Hydrochloride and 7.5% DExtrose Injection, USP) Injection of anesthetics to provide regional anesthesia

Product Classification:

Class II

Date Initiated: July 11, 2016

Date Posted: November 9, 2016

Recall Number: Z-0327-2017

Event ID: 74879

Reason for Recall:

B. Braun Medical Inc. is voluntarily recalling specific lots of their Custom Spinal Anesthesia Tray which contains a drug component, 5% Lidocaine Hydrochloride and 7.5 % Dextrose Injection, USP that Hospira Inc. has recalled because the drug product does not meet the specification for color throughout shelf life.

Status: Terminated

Product Quantity: 1704 units

Code Information:

Catalog Number: 560399 (Lot # 0061418559, 0061422389, 0061434523, 0061438084, 0061440188, 0061446168, 0061450971, 0061459227, 0061464239, Catalog Number: 560511 (Lot # 0061413435, 0061425996, 0061438393, 0061452272, 0061465310), Catalog # 560605 (0061420240, 0061429962, 0061442280, 0061449510, 0061460497, 0061471580), Catalog # 560631 (Lot# 0061438803), Catalog # 560632 (0061438818).

Distribution Pattern:

US Distribution to: AL, IL, OK, MN, MA and WI.

Voluntary or Mandated:

Voluntary: Firm initiated