FDA Medical Device Recalls (openFDA)
Mallinckrodt Manufacturing LLC: Mallinckrodt One-Way Valve, 22F x 22M, a) Part #91346 (1 piece) and b) Part #50412 (pack of 5) Used with ventilators.
- Recall number
- Z-2450-2023
- Recalling firm
- Mallinckrodt Manufacturing LLC
- Product
- Mallinckrodt One-Way Valve, 22F x 22M, a) Part #91346 (1 piece) and b) Part #50412 (pack of 5) Used with ventilators.
- Status
- Open, Classified
- Initiated
- 2023-08-08
- Posted
- 2023-09-09
- Terminated
- not on file
- Reason
- The One-Way Valve, 22F x 22M may stick and prevent or reduce the flow of ventilated air or oxygen.
- Root cause
- Under Investigation by firm
- Action
- Mallinckrodt Pharmaceuticals issued an URGENT: MEDICAL DEVICE RECALL NOTICE to its consignees on 08/08/2023 via FedEx. the notice explained the issue, risks associated with the failure, and requested the return of the device.
- Quantity
- 13,602 units
- Distribution
- Worldwide Distribution
- Lot, serial or model codes
- a) UDI/DI 10810055283460, Lot Codes: 74L2001714, 74L2001715, 74L2001716, 74M2001125, 74B2100237; b) UDI/DI 10810055283467, Lot Codes: 74L2001714, 74L2001715, 74L2001716, 74M2001125, 74B2100237
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- BZO
- Firm FEI
- 3004531588
- Firm city
- Madison
- Firm state
- WI
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28