Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,673 recalls have been distributed to Rhode Island in the last 12 months.
Showing 42881–42900 of 47,970 recalls
Recalled Item: GoPicnic Black Bean Dip & Plantain Chips Recalled by GoPicnic, Inc. Due to...
The Issue: The chocolates included in the meal kits may contain undeclared milk allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DANNON OIKOS Fruit on the Bottom GREEK NONFAT YOGURT BLUEBERRY 0% FAT...
The Issue: OIKOS Nonfat Yogurt Blueberry Flavor Single Serve 5.3 oz cups were recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gopicnic Recalled by GoPicnic, Inc. Due to Undeclared Milk
The Issue: The chocolates included in the meal kits may contain undeclared milk allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aminosyn II Recalled by Hospira Inc. Due to Presence of Particulate Matter:...
The Issue: Presence of Particulate Matter: Confirmed customer complaint of particulate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Watson...
The Issue: Defective Container: Defective bottles may not have tamper evident seals...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPIRIVA HandiHaler (Tiotropium Bromide Inhalation Powder) Capsules 18 mcg...
The Issue: Presence of Foreign Substance: This recall is being conducted due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Vision Mounting Arm Recalled by Stryker Endoscopy Due to When...
The Issue: When positioning the display located on top of the video cart, it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II Femoral Component Recalled by Zimmer, Inc. Due to The low...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Head (Not distributed in the United States) Used in Recalled by Zimmer,...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen CR-Flex Mobile Bearing Tibial Component 9 (Not distributed in...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...
The Issue: There are artifacts appearing on the Tracker images during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul¿ Head. Intended for use either with or without bone Recalled by...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay...
The Issue: Imprecision with certain lots
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Device Name: Terino Square Chin-Style II-Medium Recalled by Implantech...
The Issue: Implantech initiated a voluntary recall of certain lots of Terino Square...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multipolar¿ Bipolar Cup METAL SHELL 38 MM OD through 71 Recalled by Zimmer,...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion Set, Model#...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Femoral Component (CR-FLEX GSF POR FEM Recalled by Zimmer, Inc. Due...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ Flex Femoral Component. Provides increased flexion capability....
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.