Recall Z-0443-2019— bioMerieux, Inc.
Class II · Terminated
Class II FDA medical device recall by bioMerieux, Inc., initiated 2018-10-08, terminated 2021-05-21. FDA's recall record names no specific 510(k) clearance for this event. Product: bioM¿rieux NucliSENS easyMAG Lysis Buffer ref. 280134. Reason: Some eluates become colored because of remaining hemoglobin in the eluate..
- Recalling firm
- bioMerieux, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-10-08
- Terminated
- 2021-05-21
- Firm location
- Durham, NC, United States
Product description
bioM¿rieux NucliSENS easyMAG Lysis Buffer ref. 280134
Reason for recall
Some eluates become colored because of remaining hemoglobin in the eluate.
Data sourced from openFDA. This site is unofficial and independent of the FDA.