Becton Dickinson & Co.: Device, Gas Generating

Recall Summary BD GasPak EZ CO2 Pouch Systems (Catalog Number 260684) used in microbiology labs are being recalled because certain batches of the gas-generating sachets may not produce the correct level of carbon dioxide. The recall affects products distributed nationwide in the US and in Hong Kong.

Recalling firm
Becton Dickinson & Co.
Product
BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use
Reason
BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.
Classification
Class I
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-04-07
Status
Open, Classified
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
Worldwide distribution - US Nationwide and the country of Hong Kong.

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a760c83e-ad09-4f67-8b68-ad41c4026e06