Class IIOngoingZ-0119-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Recalls in Pennsylvania
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 373–384 of 607 recalls
Class IIOngoingZ-0118-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0117-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm)…
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0116-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm)…
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0115-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9cm)…
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IIOngoingZ-0114-2026
B BRAUN MEDICAL INC recalls PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tu…
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL INCPAOct 15, 2025
Class IOngoingZ-2668-2025
Siemens Medical Solutions USA, Inc recalls MAGNETOM Vida Fit. Model Number: 11410481.
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure…
Siemens Medical Soluti…PAOct 8, 2025
Class IOngoingZ-2667-2025
Siemens Medical Solutions USA, Inc recalls MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure…
Siemens Medical Soluti…PAOct 8, 2025
Class IOngoingZ-2666-2025
Siemens Medical Solutions USA, Inc recalls MAGNETOM Verio Dot Upgrade. Model Number: 10684334.
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure…
Siemens Medical Soluti…PAOct 8, 2025
Class IOngoingZ-2665-2025
Siemens Medical Solutions USA, Inc recalls MAGNETOM Verio Dot. Model Number: 10684333.
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure…
Siemens Medical Soluti…PAOct 8, 2025
Class IOngoingZ-2664-2025
Siemens Medical Solutions USA, Inc recalls MAGNETOM Verio. Model Number: 10276755.
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure…
Siemens Medical Soluti…PAOct 8, 2025
Class IOngoingZ-2663-2025
Siemens Medical Solutions USA, Inc recalls MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number: 10837643. 2. M…
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure…
Siemens Medical Soluti…PAOct 8, 2025