Remel Inc: Medical Device Recall in 2016 - (Recall #: Z-1921-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Oxoid Nitrocefin (+ Reconstitution Fluid Batch) REF: SR0112C, Oxoid Ltd. For the rapid chromogenic detection of beta-lactamase activity in bacterial cells. in vitro diagnostic

Product Classification:

Class II

Date Initiated: March 24, 2016

Date Posted: June 15, 2016

Recall Number: Z-1921-2016

Event ID: 73658

Reason for Recall:

Individual bottles of product may produce weak beta-lactamase reactions. Use may result in delayed or false negative reporting.

Status: Terminated

Product Quantity: 2 units were imported and distributed domestically

Code Information:

Lot 1717357 Exp: 31Aug2017

Distribution Pattern:

US distribution in MO.

Voluntary or Mandated:

Voluntary: Firm initiated