Rhode Island Recalls
2,223 recalls on record affecting Rhode Island
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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Kettle Cuisine, LLC recalls Individual Unit Label (both lid and front of cup): Whole Foo
Contains undeclared allergen (shrimp).
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The Coffee Connexion Co., Inc recalls Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag a
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
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The Coffee Connexion Co., Inc recalls Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag an
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
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The Coffee Connexion Co., Inc recalls 1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
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The Coffee Connexion Co., Inc recalls Aramark Cheese Sauce New & Improved, 25 lb., packaged in a t
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
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C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc
Due to stain present on the surface of affected foley catheters.
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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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SUNGAL INC recalls XZL, Jelly Snacks, 12.68 OZ, Bag. 12 Bags per Case.
Product Contains undeclared FD&C Yellow #5 & #6 and Red #40
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Diversatek Healthcare recalls Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dila
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
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Diversatek Healthcare recalls Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dil
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
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Diversatek Healthcare recalls Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dil
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
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Diversatek Healthcare recalls Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dil
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
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Winder Laboratories, LLC recalls Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
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Ajinomoto Foods North America Inc. recalls Item 6430153 Ajinomoto Vegetable Gyoza Dumplings. Net wt. 24
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
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Ajinomoto Foods North America Inc. recalls Item 5650893 Ajinomoto Japanese-Style Vegetable Fried Rice m
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
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Showing 20 of 2,223 recalls. Use search to filter further.