PSC Industries Inc: Medical Device Recall in 2012 - (Recall #: Z-1995-2012)

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 8.5" (215.9mm) Serrated 1.0 mm Tips Electrosurgical/Monopolar Forceps/Reusable, Model #41604, 510 (k) #K885199. The surgical device is package in non-sterile small plastic tubes. Monopolar Reusable Forceps - are intended for use in cutting and coagulating tissue during surgical procedures.

Product Classification:

Class II

Date Initiated: June 1, 2012

Date Posted: July 18, 2012

Recall Number: Z-1995-2012

Event ID: 61958

Reason for Recall:

Firm officials reported to CIN-DO that their Electrosurgical Monopolar Reusable Bayonet Forceps are misbranded in that the label states that the tip size is: (0.5mm) when the tip size actually measures (1.0mm).

Status: Terminated

Product Quantity: 5 units

Code Information:

Model/part Number: 41604, Lot Number: 019737, and 021578.

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