Drug recall

Oxoid Antimicrobial Susceptibility Test Discs, Ampicillin 10 mcg., CT0003B, packaged in cartridges of 50…

FDA recall event 65184 · Class II · Remel Inc

Key facts

Event ID 65184
Recall numbers Z-0792-2014, Z-0793-2014, Z-0794-2014, Z-0795-2014
Recalling firm Remel Inc
Product type Devices
Products Oxoid Antimicrobial Susceptibility Test Discs, Ampicillin 10 mcg., CT0003B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire…, Oxoid Antimicrobial Susceptibility Test Discs, Cefpodoxime 10 mcg., CT1612B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire…, Oxoid Antimicrobial Susceptibility Test Discs, Ertapenem 10 mcg., CT1761B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire…, Oxoid Antimicrobial Susceptibility Test Discs, Norfloxacin 10 mcg., CT0434B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire…
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Cartridges may contain individual discs which were not impregnated with antibiotic.
Initiation date Apr 9, 2013
Report date Jan 29, 2014
Termination date Jan 21, 2014
City Lenexa
State KS
Country United States
FEI number 1924669

At a glance

  • 1–9 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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