West Virginia Recalls

SDI Limited recalls Dentsply Sirona Capsule Mixer Model No. 5546068

Potential for electrical discharge from unit when unplugged.

View recall details →

Byron White Formulas, Inc. recalls Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. o

Label does not declare walnuts in English

View recall details →

Byron White Formulas, Inc. recalls Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL

Label does not declare walnuts in English

View recall details →

Byron White Formulas, Inc. recalls Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30

Label does not declare walnuts in English

View recall details →

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.

View recall details →

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.

View recall details →

Fry Pie Factory LLC recalls Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged

Undeclared allergen (milk) and process deviation (product not held under refrigeration as required)

View recall details →

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.

View recall details →

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.

View recall details →

Nutrisystem Inc recalls Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow

Undeclared Allergen (Soy)

View recall details →

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.

View recall details →

Jesse Withrow recalls My Wife's Slaw, packaged in 8 oz. and 16 oz. glass mason jar

Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified.

View recall details →