Recall Z-1982-2026— Becton Dickinson & Co.
Class II · Ongoing
Class II FDA medical device recall by Becton Dickinson & Co., initiated 2026-04-07. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Becton Dickinson & Co.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-04-07
- Firm location
- Sparks, MD, United States
Product description
BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.