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B

ird

et al

.:

J

ournal of

aoaC i

nternational

V

ol

.

99, n

o

.

4, 2016

997

butter, the isolates recovered from Laboratory 3 serotyped

as the same strain as the inoculating organism, indicating

that cross-contamination of the sample occurred. Due to

the fact that cross-contamination occurred, the data were

excluded from statistical analysis. For the statistical analysis

of each matrix, all laboratory data that were submitted were

included, with the exception of Laboratories 7 and 3 for the

creamy peanut butter. Laboratory 7 indicated difficulties in

the lysis procedure during its analysis of the creamy peanut

butter test portions. After discussions with Laboratory 7, it

was identified that an incorrect temperature was used during

the lysis procedure. The incorrect temperature was obtained

using an inappropriate thermometer for the 3M heat lysis

block insert, which resulted in the combination of sample

and lysis buffer in the lysis tubes to boil over during the heat

lysis process. Due to the fact that samples were not heated at

the proper temperature and that cross-contamination of the

samples may have occurred, data from Laboratory 7 was not

included in the statistical analysis.

Overall, the data generated during this evaluation demonstrate

reproducibility of the new method. For each matrix, the POD

statistical analysis indicated that no statistically significant

difference between the candidate method and the reference

method or between the presumptive and confirmed results of

the candidate method was obtained.

Recommendations

It is recommended that the 3M MDA 2 –

Salmonella

method

be adopted as Official First Action status for the detection of

Salmonella

in selected foods: raw ground beef (73% lean), raw

ground chicken, chicken carcass rinse, chicken carcass sponge,

pasteurized liquid whole egg, cooked breaded chicken, instant

nonfat dry milk, black pepper, cocoa powder, raw whole shrimp,

raw bagged spinach, creamy peanut butter, dry dog food,

pasteurized processed American cheese, and sealed concrete,

stainless steel, and sealed ceramic tile environmental surfaces.

Acknowledgments

We would like to extend a sincere thank you to the following

collaborators for their dedicated participation in this study:

Robert Brooks, ATC Microbiology, LLC, North Little

Rock, AR

Joel Blumfield, EDL Labs, Inc., Purvis, MS

Adam Hankins, McCoy & McCoy Laboratories, Inc.,

Madisonville, KY

Jerry Lynn Pickett, Joseph Reynolds, and Jamie Casimir,

Tyson WBAAnalytical, Springdale, AR

Leslie Thompson, VANGUARD SCIENCES, North Sioux

City, SD

Luci Hardrath, AgSource Laboratories, Marshfield, WI

Jean Schoeni and Mikiko Tillottson, Covance, Inc.,

Madison, WI

Alexandra Calle and David Campos, Texas Tech University,

Lubbock, TX

Maria Mendres and Kenneth Naylor, Now Health Group,

Bloomingdale, IL

Brian Kupski and Nicole Cuthbert, Silliker, Food Science

Center, Crete, IL

Ben Bastin and Alison Deshields, Q Laboratories Inc.,

Cincinnati, OH

Heidi Wright, AEMTEK, Inc., Fremont CA

Jesse Miller, Bryan Schindler, Eric Budge, Zach Geurin, Alex

Repeck, and Courtney Gies, NSF International, Ann Arbor, MI

Tonya Bonilla, Cynthia Zook, and Christina Barnes, 3M

Food Safety, St. Paul, MN

We would like to extend a special thanks to the following

team members at Q Laboratories, Inc. for their efforts during the

collaborative study: M. Joseph Benzinger, Jr, Allison Mastalerz,

Megan Boyle, Jonathan Clifton, T. Shane Wilson, Meghan

Daniel, and Nicole Klass.

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