Remel Inc: Medical Device Recall in 2018 - (Recall #: Z-3019-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

remel THIOGLYCOLLATE MEDIUM, REF 05152

Product Classification:

Class II

Date Initiated: August 13, 2018

Date Posted: September 19, 2018

Recall Number: Z-3019-2018

Event ID: 80813

Reason for Recall:

Products have intermittently failed performance testing during stability studies with various anaerobic microorganisms.

Status: Terminated

Product Quantity: 48 units

Code Information:

Lot number: 258192

Distribution Pattern:

US, Canada, Singapore

Voluntary or Mandated:

Voluntary: Firm initiated