Rhode Island Recalls

Merit Medical Systems, Inc. recalls Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1

The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.

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SDI Limited recalls Dentsply Sirona Capsule Mixer Model No. 5546068

Potential for electrical discharge from unit when unplugged.

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Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGIC

Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing

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Prospector Popcorn, LLC recalls Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz.

Inaccurately declared nutrients including Carbohydrates (understated) and Cholesterol (understated).

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

Label does not declare walnuts in English

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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

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

Label does not declare walnuts in English

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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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AMD Medicom Inc. recalls Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 8599

Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification for devices that contact the cerebrospinal fluid. Elevated endotoxin levels may lead to neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

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AMD Medicom Inc. recalls Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, N

Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification for devices that contact the cerebrospinal fluid. Elevated endotoxin levels may lead to neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

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