Remel Inc: Medical Device Recall in 2013 - (Recall #: Z-0808-2013)

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 Discs, Cefoxitin 30ug REF CT0119B, packaged with 50 discs per cartridge, 5 cartridges per box. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hants, UK.

Product Classification:

Class II

Date Initiated: August 21, 2012

Date Posted: February 20, 2013

Recall Number: Z-0808-2013

Event ID: 63556

Reason for Recall:

The firm is recalling the product because the cartridges may contain discs that have an insufficient dose of antibiotic.

Status: Terminated

Product Quantity: 23 units

Code Information:

Lot 1186069

Distribution Pattern:

US Nationwide Distribution including the states of: CA, CT, GA, IA, KS, OK, RI, TX, WA, WI,

Voluntary or Mandated:

Voluntary: Firm initiated