Washington Recalls
5,316 recalls on record affecting Washington
Orthofix U.S. LLC recalls Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
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Orthofix U.S. LLC recalls Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS REF:
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
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Orthofix U.S. LLC recalls Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF:
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
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Orthofix U.S. LLC recalls Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
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General Mills James Ford Bell Technical Center recalls Pillsbury Bread Rolls, Kaiser Roll Dough. 144 units / 2.5oz
Potential foreign material (glass)
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General Mills James Ford Bell Technical Center recalls Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz
Potential foreign material (glass)
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AMY'S KITCHEN INC. recalls Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ
Potential for spoilage.
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Nutricia North America recalls functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPL
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
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Nutricia North America recalls functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
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Fresh & Ready Foods LLC recalls Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.
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Fresh & Ready Foods LLC recalls Fresh to You Burger Chicken Fillet, SKU 10150, Net wt. 5oz.
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.
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MARS SNACKING recalls MorningStar Farms Hot & Spicy Sausage Patties, 100% Plant Pr
Potential contamination with plastic material
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MARS SNACKING recalls MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein
Potential contamination with plastic material
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Prime Food Processing LLC. recalls Dried Herring Fish 7 oz.
Improperly eviscerated which may result in Clostridium botulinum contamination
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Beta Bionics, Inc. recalls iLet Bionic Pancreas, REF: BB1001
The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the user successfully slides the unlock slider on the Lock Screen, no screen transition occurs, and the user remains on the Lock Screen. Because the user cannot exit the Lock Screen, the user is unable to perform a cartridge change or meal announcement. If this occurs and therapy is in progress, therapy will continue normally until the insulin cartridge is depleted. The user will be unable to perform a cartridge change or a meal announcement and will be stuck on the screen until the battery fully drains. This can lead to hyperglycemia.
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BD SWITZERLAND SARL recalls BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382
Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has led some clinical users to perceive the connection as unstable.
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Abiomed, Inc. recalls Impella CP Set with SmartAssist. Product Codes: 1000080, 100
Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical circulatory support.
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Azuma Foods International Inc USA recalls azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISH
Undeclared fish.
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U.S. Tov, Inc. dba U.S. Trading Company recalls DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz (125 g) PRO
Potential contamination with lead.
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Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump, Model Numbe
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or readily visible and the devices therefore remained in service. More specifically, drops or jarring on a hard surface can cause the touchscreen input cable to loosen, resulting in unintended touchscreen behavior on the LVP, including random screen touches and/or lack of screen responsiveness to user input. Under the reported failure condition, unintended touch inputs may register at arbitrary screen locations without user interaction. These inputs occur intermittently and without a predictable pattern.
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Showing 20 of 5,316 recalls. Use search to filter further.