Aspen Surgical Products, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1419-2014)

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:

10FR Drain Kit, Flat Full Perforated with Trocar, Saber 100ml Bulb and 3C System, Sterile (10/case) Intended for closed wound suction drainage

Product Classification:

Class II

Date Initiated: March 20, 2014

Date Posted: April 16, 2014

Recall Number: Z-1419-2014

Event ID: 67757

Reason for Recall:

The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.

Status: Terminated

Product Quantity: N/A

Code Information:

Product Number 310017

Distribution Pattern:

Worldwide Distribution - USA including LA, MA, NH, TX, FL, OH, NC, PA, CA, UT, TN, MI, CO, WY, OK, WA, MN, PA, IN, VA, IA, IL, MD, CT, DE, SC, NY, AR, MA, AZ, NJ, MO, GA, KS, WV, NE, NC, Puerto Rico, and Internationally to Canada, UAE, England, Italy, Belgium, Costa Rica, and Ecuador.

Voluntary or Mandated:

Voluntary: Firm initiated