PSC Industries Inc: Medical Device Recall in 2012 - (Recall #: Z-1996-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips, Sterile Single Use Surgical/Bipolar Forceps, Model #20-1360I, 510 (k) #K884656. The surgical device is package one (s) per plastic Tyvek peel pouch, 10 plastic Tyvek peel pouches per box. Bipolar Forceps and Cords - Olsen Medical Bipolar Forceps and Cords are intended for use in coagulating tissue during surgical procedures.

Product Classification:

Class II

Date Initiated: June 1, 2012

Date Posted: July 18, 2012

Recall Number: Z-1996-2012

Event ID: 61958

Reason for Recall:

Firm officials reported to CIN-DO that the outer carton label of this sterile, single use device is misbranded in that it lists an incorrect expiration date. The outer carton label lists the sterile expiration date as: 2012-02-(28) [the manufacture date] ; however the device pouch label lists the sterile date as: 2017-02-(28). The pouch label lists the correct sterile expiration date.

Status: Terminated

Product Quantity: 80 units

Code Information:

Model/part Number: 20-1360I, Lot Number: 023399, Expiration Date: 02/28/2017.

Distribution Pattern:

Worldwide distribution: USA (nationwide) including states of: CA, CT, FL, GA, MD, MI, NC, OR, SC, and TX and countries of: Canada and Philippines.

Voluntary or Mandated:

Voluntary: Firm initiated