FDADecember 8, 2017device
Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum, Ref R30164201 ZH01. Product Usage: Suitable for the use in slide agglutination tests to identify Shigella cultures presumptively for epidemiological and diagnostic purposes.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The serum may fail to agglutinate within the specified minimum reaction time.
What to do
FDA enforcement status: Terminated
Brands named
remel
UPCs
50560805009592
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAOxoid Agglutinating Sera, Salmonella 9-0 R309573012026-03-25
- FDAYeastone Broth, 11ML, 10/BOX YY34622026-03-24
- FDACampy CVA Medium 100/PK, R012722026-02-05
- FDA1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT34502025-11-12
- FDABlood Agar,5% Sheep Blood 100/PK, Product Number R012022025-07-11
- FDAStrep Selective II Agar, Product Number R018592025-07-11
- FDABlood/MacConkey Biplate 100/PK, Product Number R020492025-07-11
- FDABlood/EMB, Levine 100/PK, Product Number R020412025-07-11
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