Remel Inc: Medical Device Recall in 2013 - (Recall #: Z-2081-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin), Cat. #CT0036B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England Product is used in the semi-quantitative agar diffusion test method for in-vitro susceptibility testing.

Product Classification:

Class III

Date Initiated: March 25, 2013

Date Posted: September 4, 2013

Recall Number: Z-2081-2013

Event ID: 64852

Reason for Recall:

Use of affected lots may give false indication of susceptibility to Nitrofurantoin.

Status: Terminated

Product Quantity: 60 packs

Code Information:

Lots 1194944 and 1198342

Distribution Pattern:

US Distribution including the states of AL, AR, CA, FL, GA, IL, KS, LA, MA, MD, NY, OK, PA, RI, TX, VA, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated