FDA Device recall Z-1983-2026
BD GasPak EZ Campy Pouch System
- FDA Device
- Class II
- ongoing
- Published 2026-05-06
On 2026-05-06 the FDA classified a Class II recall of BD GasPak EZ Campy Pouch System by Becton Dickinson And, citing 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 leve….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1983-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-04-07 |
| Published | 2026-05-06 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BD GasPak EZ Campy Pouch System. Catalog Number: 260685. 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.
Identifiers
| code_info | Catalog Number: 260685; UDI-DI: 30382902606858; Lot Number: 5329863. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1983-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.