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Lower risk Medical device recall · FDA · Published April 7, 2026

Becton Dickinson BD GasP: CO2 Pouch System Recall - Low CO2 Levels Risk

Becton Dickinson recalls BD GasPak EZ CO2 Pouch Systems (catalog 260684) for microbiology use due to potential low carbon dioxide levels. Affected lots: 5303157, 5329857, 5329860.

🇺🇸 FDA recall #Z-1982-2026Medical deviceBecton Dickinson ›
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Contact the company

Recalling firmBecton Dickinson & Co.7 Loveton Cir · Sparks, MD 21152-9212
✎ GovInfoNow plain-language explainer

Becton Dickinson is recalling certain BD GasPak EZ CO2 Pouch Systems used in microbiology labs because the gas generating sachets might not produce enough carbon dioxide. This could affect lab results if the CO2 levels are too low. Read more at govinfonow.com/recall/49537-becton-dickinson-bd-gasp-co2-pouch-system-recall-low-co2.

Source Summary by GovInfoNow · govinfonow.com/recall/49537-becton-dickinson-bd-gasp-co2-pouch-system-recall-low-co2 · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1982-2026

Cite this page

“Becton Dickinson BD GasP: CO2 Pouch System Recall - Low CO2 Levels Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/49537-becton-dickinson-bd-gasp-co2-pouch-system-recall-low-co2. Based on FDA recall #Z-1982-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1982-2026%22&limit=1).

The Food and Drug Administration announced on April 7, 2026, that Becton Dickinson & Co. is recalling BD GasPak EZ CO2 Pouch System catalog number 260684 for microbiologic use due to potential carbon dioxide levels below specification.

How to tell if you have it

  • Brand: Becton Dickinson
  • Product: BD GasPak EZ CO2 Pouch System
  • Catalog Number: 260684
  • Lot Numbers: 5303157, 5329857, 5329860

The hazard

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.

Context

GovInfoNow's records show Becton Dickinson & Co. has 43 other recalls on record since June 1, 2017. Other recent recalls of similar products include Siemens Epoc Blood Test Cards (April 2, 2026), Abbott i-STAT EG6+ Cartridges (April 1, 2026), and BioFire Respiratory Panel 2.1 Recall (October 22, 2025).

How to tell if you have this one

Check for catalog number 260684 on the pouch system. Affected lots are 5303157, 5329857, and 5329860. The product is used in microbiology labs.

  • Brand
    Becton Dickinson
  • Category
    Medical device
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Worldwide distribution - US Nationwide and the country of Hong Kong.
Recall numberProduct, codes & lotsQuantity
Z-1982-2026BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use; Catalog Nunber: 260684; UDI-DI: 30382902606841; Lot Numbers: 5303157, 5329857, 5329860.25,760 units
Z-1983-2026BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use; Catalog Number: 260685; UDI-DI: 30382902606858; Lot Number: 5329863.2,200 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for lot numbers 5303157, 5329857, or 5329860 on the pouch system.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide distribution - US Nationwide and the country of Hong Kong.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 29 days after the firm started it.

1. Firm started the recall: Apr 7, 202612. FDA classified it Class II: Apr 29, 202623. Published in FDA’s Enforcement Report: May 6, 202632026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-1982-2026 (April 7, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1982-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA