Home › Device types › MUQ
Glue, Surgical, Arteries
FDA product code MUQ · Class 3 · Unknown
20
Registered devices
495
Adverse events
5
Recalls
0
510(k) clearances
Devices with this code
Bioglue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.BioGlue Surgical Adhesive — Artivion, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-10-07 | CryoLife, Inc. | Product is not approved for use in the EU and should not have been distributed in the EU. |
| 2021-10-05 | Siemens Medical Solutions USA, Inc | System operator manual states that the system should be rebooted once, every 7 days. In some cases, users are not following these instructions and the system is |
| 2018-06-04 | CryoLife, Inc. | The CryoLife L6318 (Label, BioGlue 12mm Spreader Tip, Indicator Label 2 1/8" x 1 1/4") was incorrectly applied to the Syringe Applicator Tip pouches and Syringe |
| 2017-05-19 | CryoLife, Inc. | The courtesy labels in 9 boxes of BioGlue were incorrectly labeled as lot 17MJX007 instead of lot 17MJX002. |
| 2014-04-25 | CryoLife, Inc. | Serum albumin component monomer failed to meet internally established end of shelf-life specification. |
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