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FDA Medical Device Recalls (openFDA)

Remel Inc: 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.

Recall number
Z-1748-2015
Recalling firm
Remel Inc
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.
Status
Terminated
Initiated
2015-05-04
Posted
2015-06-10
Terminated
2017-02-13
Reason
Product may be contaminated with Listeria monocytogenes.
Root cause
Material/Component Contamination
Action
The recalling firm sent the recall notification letter (dated May 1, 2015) to all customers on 5/4/2015 via standard mail.
Quantity
845/10/10-plate pack cases
Distribution
Nationwide Distribution.
Lot, serial or model codes
Lot Number: 646595 and 646596 Expiration date: 19May2015
510(k) numbers
not on file
PMA numbers
not on file
Product code
JSG
Firm FEI
1924669
Firm city
Lenexa
Firm state
KS
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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