FDA Medical devices recall ·
BD GasPak EZ CO2 Pouch System recall
- Recall number
- Z-1982-2026
- Date
- (initiated April 7, 2026)
- Company / brand
- Becton Dickinson & Co.
7 Loveton Cir, Sparks, MD, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 25,760 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Catalog Nunber: 260684; UDI-DI: 30382902606841; Lot Numbers: 5303157, 5329857, 5329860.
Distribution
Worldwide distribution - US Nationwide and the country of Hong Kong.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1982-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.