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. 2,390 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,390 in last 12 months

Showing 2054120560 of 47,970 recalls

DrugJuly 18, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...

The Issue: Lack of Assurance of Sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 18, 2019· Mountain Rose Inc. dba Mountain Rose Herbs

Recalled Item: Fennel Whole Seed was packaged in a clear plastic bag Recalled by Mountain...

The Issue: Fennel Whole Seed is recalled due to a potential for contamination with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 18, 2019· Arrow International Inc

Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central...

The Issue: Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2019· Medical Intelligence Medizintechnik Gmbh

Recalled Item: IGuide System Recalled by Medical Intelligence Medizintechnik Gmbh Due to...

The Issue: Sometimes, although the HexaPOD has reached the target position, the...

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

Class II — Potential Health HazardOngoing
DrugJuly 17, 2019· Macleods Pharma Usa Inc

Recalled Item: Tamsulosin Hydrochloride Capsules Recalled by Macleods Pharma Usa Inc Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2019· ImprimisRx NJ

Recalled Item: Timolol- Dorzolamide- Latanoprost P-F (0.5/2.0/0.005%) ophthalmic drops...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2019· ImprimisRx NJ

Recalled Item: Timolol-Latanoprost P-F (0.5/0.005%) ophthalmic drops Recalled by ImprimisRx...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream USP100 Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out-of-specification result...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Viral Panel RUO Recalled by Becton Dickinson & Co. Due to...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max StaphSR Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 1 USA Recalled by Becton Dickinson & Co. Due to The foil...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit EXT Enteric Bacterial Panel Recalled by Becton Dickinson & Co. Due to...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Check-Points CPO IVD EU Recalled by Becton Dickinson & Co. Due to...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Viral Panel EU Catalog # 443985 Recalled by Becton...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK TNA 2 Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 1 EU LUO Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max MRSA Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Vaginal Panel Recalled by Becton Dickinson & Co. Due to The foil...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 2 EU LUO Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max StaphSR Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing