Loading...
Loading...
All product recalls associated with Remel Inc.
Total Recalls
45
Past Year
9
Class I (Serious)
0
Most Recent
Nov 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The media allows growth of E. faecalis ATCC 29212 with blackening of the media.
When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may exhibit lighter than normal growth making zones difficult to measure.
The blood agar side of the bi-plate may not grow some patient isolates or QC organisms as intended.
Use of the product could result in inadequate recovery of Legionella pneumophila which could result in false negative reporting.
The product may appear cloudy or discolored and may not perform correctly in presumptive diagnosis of mycobacterial disease.
A reagent within the test may return false negative results.
A reagent within the test may return false negative results.
Recalled product may not provide adequate recovery of Legionella pneumophila when used as directed and may result in false negative identification of Legionella pneumophila.
Product failure - Failure to grow quality control strains of Streptococcus pneumoniae.
The product may fail to adequately grow methicillin resistant Staphylococcus aureus ATCC 43300 and Staphylococcus aureus ATCC 33591.
There is an error in Version 1.0.77 of the electronic code compendium (ERIC) software. The error is limited to the database corresponding to the R8311007 RapID Yeast Plus System. The database erroneously includes Candida dubliniensis as well as displays an incorrect temperature range as an accessory test for codes with an overlap between Candida albicans and Candida dubliniensis. When using the
The products may give false positive results with some non-Staphylococcus aureus strains
The products may give false positive results with some non-Staphylococcus aureus strains
Incorrect expiration date on the product
The plate labeling is incorrect, but the outer box labeling is correct
These lots may exhibit false positive reactions with strains of Staphylococcus epidermidis that may result in the mis-identification of Staphylococcus aureus.
Control and test wells are reversed on some of the reaction cards.
Faint grey test lines for Cryptosporidium may be visible which may be interpreted as false positive
Failure to produce reaction: Use of the product with various RapID Identification systems panels may exhibit poor or no reactions.
False negative results for sorbitol fermenting bacteria such as E. Coli 0157.