Gibson Laboratories LLC: Medical Device Recall in 2018 - (Recall #: Z-0606-2018)

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:

Blastomyces dermatitidis Antiserum 1 mL vial GIBSON BIOSCIENCE. Catalog 200265 Intended for identification of the systemic fungal pathogens.

Product Classification:

Class II

Date Initiated: January 20, 2017

Date Posted: February 21, 2018

Recall Number: Z-0606-2018

Event ID: 78731

Reason for Recall:

The firm information that the product was reporting false positive results

Status: Terminated

Product Quantity: 10/1 mL vials

Code Information:

Lot # 5072543 Exp Date 03/12/2021; UDI : 10634853000039.

Distribution Pattern:

Distributed to the states of AL, AZ & MS.

Voluntary or Mandated:

Voluntary: Firm initiated