Medical Device Recalls
-
1 to 5 of 129 Results
Product: pio |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
SIGNA Pioneer, with affected software versions: PX25.0 to PX25.5, PX26.0, PX26.1, PX28.0 to PX28.4,... | 2 | 08/02/2024 | GE Medical Systems, LLC |
Capio SLIM Suture Capturing Device, Box of 5, Outer Package UPN: M0068318261, Inner Package UPN: M00... | 2 | 07/30/2024 | Boston Scientific Corporation |
Capio SLIM Suture Capturing Device, 1-Pack, UPN: M0068318250. Capio SLIM Suture Capturing Devices a... | 2 | 07/30/2024 | Boston Scientific Corporation |
SCORPIO RECESSED PATELLA- Intended for Knee Replacement Part Number: 3044-0026 | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
Scorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Part Number: 82-2-0910 ... | 2 | 01/31/2024 | Howmedica Osteonics Corp. |
-