Customed, Inc: Medical Device Recall in 2015 - (Recall #: Z-2554-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

MAJOR LAPAROTOMY PK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .

Product Classification:

Class II

Date Initiated: July 10, 2015

Date Posted: September 9, 2015

Recall Number: Z-2554-2015

Event ID: 71721

Reason for Recall:

Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.

Status: Terminated

Product Quantity: 1084 packs

Code Information:

Catalog number:900036 Lots: 141015515 exp. 11/30/15 141015515 exp. 11/30/15 141216311 exp. 12/31/15 150116932 exp. 1/31/16 150116931 exp. 1/31/16 150116935 exp. 1/31/16 150116934 exp. 1/31/16 150116933 exp. 1/31/16 150217245 exp. 1/31/16 150217246 exp. 1/31/16 150217247 exp. 1/31/16 150317571 exp. 3/31/16 150317572 exp. 3/31/16 150317573 exp. 3/31/16 150317575 exp. 4/30/16 150317574 exp. 4/30/16 150418256 exp. 4/30/16 150418256 exp. 4/30/16 150418257 exp. 4/30/16 150418258 exp. 4/30/16 150418259 exp. 4/30/16 150518615 exp. 5/31/16 150518616 exp. 5/31/16 150518616 exp. 5/31/16 150519020 exp. 5/31/16 150519019 exp. 5/31/16

Distribution Pattern:

Distributed Only in Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated