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 1070110720 of 47,970 recalls

FoodOctober 7, 2022· Flowers Foods (Corporate Offices)

Recalled Item: TASTYKAKE GLAZED APPLE PIE NET WT 4.5 OZ (128g) Recalled by Flowers Foods...

The Issue: During an internal inspection the firm discovered that several products may...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2022· Ferno-Washington Inc

Recalled Item: FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V...

The Issue: Batteries could become unstable when not properly maintained and/or...

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

Class II — Potential Health HazardOngoing
DrugOctober 6, 2022· Golden State Medical Supply Inc.

Recalled Item: Rifampin Capsules Recalled by Golden State Medical Supply 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
DrugOctober 6, 2022· Golden State Medical Supply Inc.

Recalled Item: Rifampin Capsules Recalled by Golden State Medical Supply 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 DeviceOctober 6, 2022· Edwards Lifesciences, LLC

Recalled Item: Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP...

The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2022· Edwards Lifesciences, LLC

Recalled Item: Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP...

The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...

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

Class II — Potential Health HazardOngoing
DrugOctober 5, 2022· Aurobindo Pharma USA Inc.

Recalled Item: Quinapril and Hydrochlorothiazide Tablets Recalled by Aurobindo Pharma USA...

The Issue: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 4, 2022· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

The Issue: Defective Container: Complaints received of vial breakage and glass flying...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 4, 2022· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

The Issue: Defective Container: Complaints received of vial breakage and glass flying...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 3, 2022· Beckman Coulter, Inc.

Recalled Item: MicroScan autoSCAN-4 Instrument Recalled by Beckman Coulter, Inc. Due to Due...

The Issue: Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995)...

The Issue: Due to partial label detachment on tubes. This can cause tubes to become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Trucount Tubes (Cat. No. 663028) Recalled by Becton, Dickinson and...

The Issue: Due to partial label detachment on tubes. This can cause tubes to become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Rebiscan, Inc.

Recalled Item: Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for...

The Issue: Unable to charge the battery pack- battery packs will allow the batteries to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Trucount Tubes (Cat. No. 340334) Recalled by Becton, Dickinson and...

The Issue: Due to partial label detachment on tubes. This can cause tubes to become...

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

Class II — Potential Health HazardOngoing
DrugSeptember 30, 2022· AuroMedics Pharma LLC

Recalled Item: Fondaparinux Sodium Injection Recalled by AuroMedics Pharma LLC Due to...

The Issue: Subpotent Drug: Out of specification for assay

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2022· VistaPharm, Inc.

Recalled Item: Pyridostigmine Bromide Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: cGMP Deviations: Out of specification for assay of one of the preservative...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2022· Ingenus Pharmaceuticals Llc

Recalled Item: Flunisolide Nasal Solution Recalled by Ingenus Pharmaceuticals Llc Due to...

The Issue: Out of specification for related substances (impurities).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 30, 2022· Boston Scientific Corporation

Recalled Item: EMBLEM MRI S-ICD Recalled by Boston Scientific Corporation Due to There is...

The Issue: There is an incorrect manufacturing date/timestamp within the software which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE DENTAL PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O Recalled by...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing