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North Dakota Recalls
2,153 recalls on record affecting North Dakota
Pepsico Inc recalls 28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatora
Undeclared Yellow No. 6 and/or Yellow No. 5
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Bard Access Systems, Inc. recalls DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150
this is a downstream recall of class I recall RES 98777
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BD SWITZERLAND SARL recalls BD Alaris Pump Infusion Sets 10561554* 10885403232565 508854
Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.
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Bard Access Systems, Inc. recalls Power-Trialysis Short-Term Straight Dialysis Catheter, REF:
this is a downstream recall of class I recall RES 98777
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Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Tangerine, 6-Count 2.5 ounce, with UPC 0
Foreign object: products may contain glass pieces
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Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine.
Foreign object: products may contain glass pieces
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Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UP
Foreign object: products may contain glass pieces
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Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC
Foreign object: products may contain glass pieces
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Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 04154
Foreign object: products may contain glass pieces
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Dreyer's Grand Ice Cream Inc. recalls Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 04
Foreign object: products may contain glass pieces
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Argon Medical Devices, Inc recalls L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/aspirate catheter, catheter occlusion, therapy interruption, blood loss, tissue irritation, bloodstream infection.
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Argon Medical Devices, Inc recalls L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 38462
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/aspirate catheter, catheter occlusion, therapy interruption, blood loss, tissue irritation, bloodstream infection.
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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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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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Nutrisystem Inc recalls Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow
Undeclared Allergen (Soy)
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Draeger, Inc. recalls Atlan A350. Model Number: 8211500. anesthesia workstation
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
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Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic endoscope.
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Draeger, Inc. recalls Atlan A350XL. Model Number: 8621600. anesthesia workstation
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
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Pork King Good, LLC recalls Pork King Good Onion & Sour Cream Seasoning. Net Wt. 3 oz (
Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination.
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Showing 20 of 2,153 recalls. Use search to filter further.