Snoqualmie Gourmet Ice Cream Recalls

Cherry Vanilla Custard (with egg) is being recalled due to the potential to be contaminated with Listeria monocytogenes.

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Cranberry Raspberry Sorbet (Snoqualmie) – Listeria contamination (2014)

Cranberry Raspberry Sorbet is being recalled due to the potential to be contaminated with Listeria monocytogenes

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Grapefruit Sorbet (Snoqualmie) – Listeria Contamination (2014)

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Listeria

Grapefruit Sorbet is being recalled due to the potential to be contaminated with Listeria monocytogenes

Class IHigh

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Lemon Sorbet with Swirl (Snoqualmie) – Listeria contamination (2014)

Lemon Sorbet with Lemon Swirl is being recalled due to the potential to be contaminated with Listeria monocytogenes

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Blackberry Sorbet, sold under Snoqualmie brand. Product ... (Snoqualmie Gourmet Ice Cream) – Listeria contamination (2014)

Blackberry Sorbet is being recalled due to the potential to be contaminated with Listeria monocytogenes

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Guava Sorbet (Snoqualmie) – Listeria Contamination (2014)

Guava Sorbet is being recalled due to the potential to be contaminated with Listeria monocytogenes

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Meyer Lemon Sorbet (Snoqualmie) – Listeria risk (2014)

Lemon Meyer Sorbet (Meyer Lemon) is being recalled due to the potential to be contaminated with Listeria monocytogenes

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Coconut Rum Sorbet, sold under Snoqualmie brand. Product... (Snoqualmie Gourmet Ice Cream) – Listeria contamination (2014)

Coconut Rum Sorbet is being recalled due to the potential to be contaminated with Listeria monocytogenes

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Coconut Sorbet, sold under Snoqualmie brand. Product is ... (Snoqualmie Gourmet Ice Cream) – Listeria contamination (2014)

Coconut Sorbet is being recalled due to the potential to be contaminated with Listeria monocytogenes

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Passion Fruit Sorbet, sold under Snoqualmie brand. Produ... (Snoqualmie Gourmet Ice Cream) – Listeria contamination (2014)

Passion Fruit Sorbet is being recalled due to the potential to be contaminated with Listeria monocytogenes.

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

10% Soft-Serve Vanilla Ice Cream Mix, sold under Snoqualm... (Snoqualmie Gourmet Ice Cream) – Listeria contamination (2014)

10% Soft-Serve Vanilla Ice Cream Mix is being recalled because finished product tested positive for Listeria monocytogenes.

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Ice Cream products, total 177 different flavors. Product... (Snoqualmie Gourmet Ice Cream) – Listeria contamination (2014)

All 177 flavors ice cream products are being recalled due to the potential to be contaminated with Listeria monocytogenes.

FDADec 21, 2014Nationwide• Snoqualmie Gourmet Ice Cream

Becton Dickinson & Company: BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannu...

The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the syringe.

FDADec 19, 2014Nationwide• Becton Dickinson & Company

Philips Medical Systems, Inc.: Philips IntelliVue Information Center iX (release A.00, A...

Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled without visual notification

FDADec 19, 2014Nationwide• Philips Medical Systems, Inc.

BD Biosciences, Systems & Reagents: CD8 (Leu-2a) PE (In vitro diagnostic), Catalog number 340...

One lot of CD8 PE is contaminated with CD4 FITC and may cause an unexpected staining pattern and incorrect patient data.

FDADec 19, 2014Nationwide• BD Biosciences, Systems & Reagents

BD Biosciences, Systems & Reagents: Anti-Lambda APC-H7, Catalog Number 656157. Product U...

Two lots of the Anti-Lambda APC-H7 antibody are contaminated with CD38 antibody.

FDADec 19, 2014Nationwide• BD Biosciences, Systems & Reagents

Circuit Breakers (Schneider Electric) – electrical safety (2014)

Fire/Burn Risk

The recall involves PowerPact J-frame molded case circuit breakers with thermal-magnetic trip units. The circuit breakers are made of black plastic and have a three-position breaker handle that indicates whether the breaker is off, on or tripped. The recalled circuit breakers are rated for 150 to 250 amps, have interruption ratings of D, G, J, L and R. They were manufactured in two pole and three pole configurations with either lug-in/lug-out or plug-in (I-Line) style connectors. Brand name "Schneider Electric" or "Square D" is on a yellow sticker above the breaker handle and on the top of a label on the side of the circuit breaker. A label on the front of the circuit breaker to the left of the breaker handle has the catalog number at the top. The number also appears on a label on the side of the breaker. Schneider Electric catalog numbers begin with "NJ" and Square D catalog numbers begin with "J." A label on the front of the circuit breaker to the right of the breaker handle has the date code in the lower right corner. Recalled circuit breakers were manufactured from March 26, 2014 through September 26, 2014 and have date codes 14131 through 14395. The date codes are in the YYWWD format (example: 14131 = year 2014, week 13, day of the work week 1/ Monday). Breakers with following catalog numbers are being recalled: Catalog Number Breaker Type (N)JDX26XXX 2 Pole (N)JGX26XXX 2 Pole (N)JJX26XXX 2 Pole (N)JLX26XXX 2 Pole (N)JDX36XXX 3 Pole (N)JGX36XXX 3 Pole (N)JJX36XXX 3 Pole (N)JLX36XXX 3 Pole (N)JRX36XXX 3 Pole

CPSCDec 18, 2014Nationwide• Schneider Electric USA Inc., of Columbia, Mo., and Tlaxcala, Mexico

St Jude Medical Cardiac Rhythm Management Division: Merlin@home RF Remote Monitoring Transmitter, Model EX115...

Transmitter may initiate a software reset resulting in backup operation in some implanted St. Jude Medical Radio Frequency (RF) enabled Implantable Cardioverter Assura, Unify Assura, and Quadra Assura ICDs and Assurity and Allure Pacemakers.

FDADec 18, 2014Nationwide• St Jude Medical Cardiac Rhythm Management Division

Entertainer's Secret Throat Relief (Tropichem) - microbial contamination (2014)

E. coli

Microbial Contamination of Non Sterile Product; microbial assay reported unacceptable high plate counts and positive for E. Coli

FDADec 17, 2014IN, NY• Tropichem Research Labs, Inc.

Leica Microsystems, Inc.: Liquid Mouse Monoclonal Antibody CD15 used is laboratorie...

The staining intensity decreases over the shelf life.