FDA Device recall Z-1748-2015
Remel Blood Agar (TSA w/sheep blood) plate REF R01202 packaged 10 plates per pack, 10/10-packs per case (100 plates)
- FDA Device
- Class II
- terminated
- Published 2015-06-17
On 2015-06-17 the FDA classified a Class II recall of Remel Blood Agar (TSA w/sheep blood) plate REF R01202 packaged 10 plates per pack, 10/10-packs per case (100 plates) by Remel, citing product may be contaminated with Listeria monocytogenes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1748-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-05-04 |
| Published | 2015-06-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Remel |
| Distribution | US |
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.
Identifiers
| code_info | Lot Number: 646595 and 646596 Expiration date: 19May2015 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1748-2015%22
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