AGFA Healthcare Corp.: Medical Device Recall in 2014 - (Recall #: Z-2178-2014)

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:

Radiomat M+ NIF 14 x 17; Radiomat SG 14 x 17 NIF; RX-B 8 x 10 in./IBF-004355; Radiomat B+ NIF 14 x 17; Radiomat B+ NIF 8 x 10; Radiomat B+ NIF 9 1/2 x 9 1/2; CX Ultra UV-G Plus NIF 11 x 14; Radiomat G Plus 14 x 17 NIF Product Usage: Radiographic film is a device that consists of a thin sheet of radiotransparent material coated on one or both sides of the film, with a radiotransparent material coated on one or both sides of the film, with a photographic emulsion intended to record images during diagnostic radiologic procedures.

Product Classification:

Class III

Date Initiated: July 16, 2014

Date Posted: August 20, 2014

Recall Number: Z-2178-2014

Event ID: 68844

Reason for Recall:

Some sheets of the medical screen film are fogged.

Status: Terminated

Product Quantity: 2617

Code Information:

Lot Batch No. 79350052, 79380052, 79390074, 79400066, 79410063

Distribution Pattern:

Worldwide Distribution and US Nationwide in the states of AL, AZ, CA, FL, IL, LA, MI, MN, MS, NE, NH, NJ, NC and country of Canada

Voluntary or Mandated:

Voluntary: Firm initiated