Washington D.C. Recalls — Product Safety Alerts Affecting DC

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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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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Kettle Cuisine, LLC recalls Individual Unit Label (both lid and front of cup): Whole Foo

Contains undeclared allergen (shrimp).

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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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French Broad Chocolate Factory recalls french broad CHOCOLATE bette's bake sale (a multi-flavor bon

Undeclared nut allergen (walnut) due to mislabeling. The product's printed tasting guide incorrectly identifies the Walnut Fudge and Peach Cobbler flavor chocolates (bonbons). Consumers relying on the printed materials could mistakenly consume a nut-containing bonbon.

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Elekta, Inc. recalls Brand Name: Leksell Vantage Arc System REF: 1053958

Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.

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Stryker Sustainability Solutions recalls Stryker Sustainability Solution Color Cuff 24" (Yellow) Quic

Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.

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Lidl US TRADING recalls Favorina Chocolate Ladybugs German-Style Nougat, Net Wt 3.52

Label does not specify type of tree nut contained in the product.

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JFE FRANCHISING INC recalls " Dumpling Party Tray (20pcs) Vegetable 13 oz

Foreign Object (Glass)

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JFE FRANCHISING INC recalls " Dumpling Vegetable 4.5 oz

Foreign Object (Glass)

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GE Healthcare, LLC recalls Prestige II