Recall Z-1748-2015— Remel Inc
Class II · Terminated
Class II FDA medical device recall by Remel Inc, initiated 2015-05-04, terminated 2017-02-13. FDA's recall record names no specific 510(k) clearance for this event. Product: Remel Blood Agar (TSA w/sheep blood) plate REF R01202 packaged 10 plates per pack, 10/10-packs per case (100 plates). Blood agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic reactions.. Reason: Product may be contaminated with Listeria monocytogenes..
- Recalling firm
- Remel Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-05-04
- Terminated
- 2017-02-13
- Firm location
- Lenexa, KS, United States
Product description
Remel Blood Agar (TSA w/sheep blood) plate REF R01202 packaged 10 plates per pack, 10/10-packs per case (100 plates). Blood agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic reactions.
Reason for recall
Product may be contaminated with Listeria monocytogenes.
Data sourced from openFDA. This site is unofficial and independent of the FDA.