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CHX Plus
Vista Dental · Model 502925 · UDI-DI 10818207020328
KJJ
Prescription
10
510(k) clearances
24
Adverse events
7
Recalls
35
Facilities
Description
Contains 2% Chlorhexidine Gluconate plus powerful wetting agents and proprietary surface modifiers to improve the depth of penetration. Use prior to restorative preparations of crowns and composites. Endo kit includes (4) 1.2 mL prefilled syringes & (20) 27ga side-vent irrigating tips.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-06-27 | Inter-Med Llc | The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and ex |
| 2019-06-27 | Inter-Med Llc | The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and ex |
| 2019-06-27 | Inter-Med Llc | The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and ex |
| 2019-06-27 | Inter-Med Llc | The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and ex |
| 2019-06-27 | Inter-Med Llc | The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and ex |
| 2019-06-27 | Inter-Med Llc | The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and ex |
| 2019-06-27 | Inter-Med Llc | The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and ex |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
