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. 2,515 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,515 in last 12 months

Showing 1076110780 of 47,970 recalls

FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Lyons Ready Care Thickened Orange Nectar packaged in combi-bloc multi...

The Issue: Indication of product spoilage

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Imperial Thickened Cranberry Cocktail Nectar packaged in combi-bloc multi...

The Issue: Indication of product spoilage

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Imperial Thickened Apple Honey Nectar packaged in combi-bloc multi wall...

The Issue: Indication of product spoilage

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Imperial Thickened Cranberry Cocktail Honey packaged in combi-bloc multi...

The Issue: Indication of product spoilage

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Lyons Ready Care Thickened Apple Honey Nectar packaged in combi-bloc...

The Issue: Indication of product spoilage

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Lyons Ready Care Thickened Cranberry Honey Nectar packaged in combi-bloc...

The Issue: Indication of product spoilage

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Lyons Ready Care Thickened Sweet Tea with Lemon Nectar packaged Recalled by...

The Issue: Indication of product spoilage

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Lyons Ready Care Thickened Cranberry Nectar packaged in combi-bloc multi...

The Issue: Indication of product spoilage

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Lyons Ready Care Thickened Apple Juice packaged in combi-bloc multi Recalled...

The Issue: Indication of product spoilage

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Lyons Ready Care Thickened Apple Nectar packaged in combi-bloc multi...

The Issue: Indication of product spoilage

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 23, 2022· GAGA PRO LIGHTING EQUIPMENT CO.,

Recalled Item: GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Recalled by...

The Issue: GAGA Pro LLS systems was not in compliance with the FDA's Performance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2022· LumiraDx

Recalled Item: LumiraDx SARS-CoV-2 Antigen (Ag) Liquid Quality Control Kit Catalog #:...

The Issue: Assigned vial lot numbers for the incorrect type of product. SARS-CoV-2 &...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 22, 2022· Hamilton Medical AG

Recalled Item: Hamilton-C6 Recalled by Hamilton Medical AG Due to Due to a malfunction...

The Issue: Due to a malfunction related to the backlight on the ventilator screen. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2022· ZOLL Circulation, Inc.

Recalled Item: AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model...

The Issue: Due to increase in Li-Ion Battery failures

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 21, 2022· Viatris Inc

Recalled Item: Ampicillin for Injection Recalled by Viatris Inc Due to Presence of...

The Issue: Presence of Particulate Matter: A complaint was received for the presence of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2022· Akorn, Inc.

Recalled Item: Rifampin Capsules Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2022· Akorn, Inc.

Recalled Item: Rifampin Capsules Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 21, 2022· MICROVENTION INC.

Recalled Item: WEB Detachment Controller Recalled by MICROVENTION INC. Due to Detachment...

The Issue: Detachment controller, of an aneurysm embolization system, has an out of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2022· W L Gore & Associates, Inc.

Recalled Item: GORE CARDIOFORM ASD Occluder. cardiovascular implant. Recalled by W L Gore &...

The Issue: Due to manufacturing records (Release Test Results) indicating "Failed".

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 20, 2022· QuVa Pharma, Inc.

Recalled Item: oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride...

The Issue: Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund