Fresh Recalls

FDAClass II · Medical device · Recall Z-1982-2026 · Recalled May 6, 2026

BD GasPak EZ CO2 Pouch System recall — Becton Dickinson & Co.

Agency report date: May 6, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
BD GasPak EZ CO2 Pouch System
Company / brand
Becton Dickinson & Co
Lot / serial / date codes
Catalog Nunber: 260684; UDI-DI: 30382902606841; Lot Numbers: 5303157, 5329857, 5329860.
Distribution
Worldwide distribution - US Nationwide and the country of Hong Kong.
Agency product description and boundaries

BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: BD GasPak EZ CO2 Pouch System recall status

3. Open the official notice or contact

Official recall ID
Z-1982-2026
Brand
All Becton Dickinson & Co recalls
Classification
Class II
Units affected
25,760 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Sparks, MD, United States
Firm address
7 Loveton Cir, 21152-9212

Identifying details (verbatim from the notice)

Product codes / lots
Catalog Nunber: 260684; UDI-DI: 30382902606841; Lot Numbers: 5303157, 5329857, 5329860.
Distribution
Worldwide distribution - US Nationwide and the country of Hong Kong.
Firm notified the public via
Letter
FDA event ID
98657
Recall initiated
April 7, 2026
FDA classified
April 29, 2026
FDA report date
May 6, 2026

Other medical device recalls from around the same time

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved August 4, 2026 at 11:00 PM UTC.

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