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Oregon Recalls
4,756 recalls on record affecting Oregon
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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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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Medela Inc recalls Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery of enteral nutritional fluids or oral medication.
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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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Utz Quality Foods, LLC recalls 2.5oz , 8oz , Zapp's Brand Bayou Blackened Ranch Potato Chi
Potential presence of Salmonella.
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Utz Quality Foods, LLC recalls 1.5oz, 8.0oz , Zapp's Big Cheezy Potato Chips, Plastic Bag.
Potential presence of Salmonella.
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Utz Quality Foods, LLC recalls 2.0 oz Dirty Maui Onion Chip, Plastic Bag.
Potential presence of Salmonella.
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Utz Quality Foods, LLC recalls 1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag
Potential presence of Salmonella.
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Utz Quality Foods, LLC recalls 2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.
Potential presence of Salmonella.
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Utz Quality Foods, LLC recalls 1.5oz, 2oz Dirty Brand Salt and Vinegar Potato Chips , Plast
Potential presence of Salmonella.
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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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Showing 20 of 4,756 recalls. Use search to filter further.