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. 2,262 recalls have been distributed to Rhode Island in the last 12 months.
Showing 46561–46580 of 47,970 recalls
Recalled Item: Costa Four Bean Salad 4.50 lbs Poly Tub (Item #01385 Green Beans Recalled by...
The Issue: Products contain recalled Gill's Onions due to Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Costa: 1/2" Diced Onions (Item #C228) Recalled by Fresh Ideas Inc. Due to...
The Issue: Products contain recalled Gill's Onions due to Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Costa Multiple Bean Salad 4.5 lbs Poly Tub (Item #01407) Recalled by Fresh...
The Issue: Products contain recalled Gill's Onions due to Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Eon Mini - 3788 (IPG) Recalled by St. Jude Medical Due to As part of St....
The Issue: As part of St. Jude Medical's routine tracking and product monitoring, they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Recalled by...
The Issue: St. Jude Medical has informed your doctor that a number of cases have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon Mini - 3721 (Charger). Product Usage: Eon Mini system Recalled by St....
The Issue: St. Jude Medical has informed your doctor that a number of cases have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FRx 861304 Automated External Defibrillator Manufactured...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips and Laerdal brands of HeartStart HS1 Defibrillator Family Model...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Styker Orthobiologics Vita Plasma Separator Recalled by Stryker...
The Issue: When preparing plasma using VitaPrep, it was reported that a small amount of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Serial interface module RS-232 Product Usage: The System 1 provides Recalled...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interface module for CDl System 500 Product Usage: The Interface Recalled by...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interface module for CDl System 100/101 Product Usage: The Interface...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Serial interface module RS-485 Product Usage: The System 1 provides Recalled...
The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: Subpotent; 9-month stability interval
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc. of Iowa Due...
The Issue: Subpotent; 9-month stability interval
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.075 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...
The Issue: Subpotent; 9-month stability interval
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyro-Tab 0.050 mg. Recalled by Lloyd Inc. of Iowa Due to Subpotent; 9-month...
The Issue: Subpotent; 9-month stability interval
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Topiramate Tablets Recalled by American Health Packaging Due to Labeling:...
The Issue: Labeling: Label Mix-Up: A typographical error in the product form on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.