Class IIOngoingZ-0212-2026
Biomet, Inc. recalls BIOMET ZipTight
There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop
Biomet, Inc.INOct 29, 2025
Recalls: Under Investigation by firm
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 613–624 of 1,125 recalls
Class IIOngoingZ-0205-2026
Diagnostica Stago, Inc. recalls Product: STA Liatest D-Di
A potential risk of underestimation of D-Dimer (D-Di) levels with the two listed lots.
Diagnostica Stago, Inc…NJOct 22, 2025
Class IIOngoingZ-0147-2026
Ethicon Endo-Surgery Inc recalls ECHELON LINEAR Cutters Reload 80 mm Blue
The devices were shipped unsterilized.
Ethicon Endo-Surgery I…OHOct 22, 2025
Class IOngoingZ-0035-2026
CareFusion 303, Inc. recalls BD Alaris Pump Infusion Sets for the following reference numbers: C24101E
Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion…
CareFusion 303, Inc.CAOct 15, 2025
Class IIOngoingZ-2671-2025
BioMerieux, Inc. recalls VITEK¿ 2 Gram-negative AST Test Kits (Cards) containing Colistin formulation cs02n.…
Potential for false resistant results for Colistin (cs02n) with multi-drug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii complex used in specific cards
bioMerieux, Inc.NCOct 8, 2025
Class IOngoingZ-2670-2025
Medline Industries, LP recalls Medline Kits: 1) VALVE PACK-LF
The kits contain certain lots of cannula products where the catheter may not retain its shape.
Medline Industries, LPILOct 8, 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