Dako Denmark A S recalls
Dako Denmark A S appears in 3 official U.S. recall notices indexed by RecallRadar, most recently on 2020-05-27.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 3 |
|---|---|
| Published | 2012-12-26 to 2020-05-27 |
| By agency | FDA Device (3) |
| By classification | Class II (3) |
| By status | terminated (3) |
| Distribution named in notices | US |
Recalls
- Dako Autostainer instruments: Autostainer Link 48, Model AS480
FDA Device · Class II · 2020-05-27 · Dako Denmark A S
Reason: The Autostainer instrument may not have a syringe tray installed which could result in a small volume of excess buffer being applied to several slides. In addition to the syringe tray, the updated Basic User Guide will… - EnVision FLEX+, Mouse, High pH (Link), Product No. K8002, K8004
FDA Device · Class II · 2016-08-10 · Dako Denmark A S
Reason: The pH of Target Retrieval Solution in the kit measures 4-5 instead of the correct pH of 9.1. - CoverStainer Slide Rack The CoverStainer Slide Rack is an accessory to the CoverStainer instrument
FDA Device · Class II · 2012-12-26 · Dako Denmark A S
Reason: The expected life time of the CoverStainer slide racks (CS 10330) does not meet established performance requirements, originating from variations in the manufacturing process.