Medical Action Industries Inc: Medical Device Recall in 2014 - (Recall #: Z-1951-2014)

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:

Laceration/Suture Removal, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.

Product Classification:

Class II

Date Initiated: June 12, 2014

Date Posted: July 9, 2014

Recall Number: Z-1951-2014

Event ID: 68564

Reason for Recall:

Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.

Status: Terminated

Product Quantity: 474 cs (9,480 ea) total for all kits involved

Code Information:

Model number: 72347, Lot number: 187172, Exp. Date: 9/1/2015.

Distribution Pattern:

Distributed in the states of AR, AZ, FL, GA, IA, IL, KY, MA, MN, NC, NY, OH, TN, TX, and VA.

Voluntary or Mandated:

Voluntary: Firm initiated