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. 2,326 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,326 in last 12 months

Showing 3580135820 of 47,970 recalls

Medical DeviceJuly 7, 2015· C.R. Bard, Inc.

Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2015· C.R. Bard, Inc.

Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2015· C.R. Bard, Inc.

Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...

The Issue: Potential breach of the sterile barrier packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2015· Aesculap, Inc.

Recalled Item: S4C Occiput Torque Wrench F/Set Screw Recalled by Aesculap, Inc. Due to A...

The Issue: A FW103R torque wrench that was improperly reassembled after reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2015· Eizo Corporation

Recalled Item: RadiForce RX850 Recalled by Eizo Corporation Due to EIZO is recalling the...

The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2015· Eizo Corporation

Recalled Item: RadiForce GX540 Recalled by Eizo Corporation Due to EIZO is recalling the...

The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2015· Eizo Corporation

Recalled Item: RadiForce RX650 Recalled by Eizo Corporation Due to EIZO is recalling the...

The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...

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

Class II — Potential Health HazardOngoing
DrugJuly 6, 2015· BioComp Pharma, Inc.

Recalled Item: Maximum Strength Analgesic Thera-Gesic Pain Relieving Creme Relief from:...

The Issue: Subpotent Drug: menthol and methyl salicylate below specification

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 6, 2015· Philips Electronics North America Corporation

Recalled Item: SENSE Body Coil 1.5T with identification Recalled by Philips Electronics...

The Issue: Wrong positioning of the coil cables can create unintended resonances via...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2015· Philips Electronics North America Corporation

Recalled Item: Actuator for angiographic x-ray monitor ceiling suspension system. Actuator...

The Issue: The actuator assembly became detached and the monitor carriage with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Potential...

The Issue: Potential issue leading to data loss and patient data mix-up

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2015· CooperSurgical, Inc.

Recalled Item: Infant Heel Warmer and Infant Gel Warmer Recalled by CooperSurgical, Inc....

The Issue: Product marketed without a 510(k)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2015· NordicNeuroLab AS

Recalled Item: nordicICE v 2.3.14 nordicICE is an image processing software package...

The Issue: The bug causes BOLD activation maps to be visualized as overlays without...

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

Class II — Potential Health HazardOngoing
DrugJuly 2, 2015· XTREME Z DISTRIBUTORS INC

Recalled Item: Zero Xtreme High Performance Fat Burner capsules Recalled by XTREME Z...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 2, 2015· Bestco, Inc.

Recalled Item: CVS SUGAR FREE BLACK CHERRY COUGH DROPS (MENTHOL-COUGH SUPPRESSANT) Recalled...

The Issue: Presence of Foreign Tablets/Capsules: Presence of comingled Sugar Free Honey...

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

Class III — Low RiskOngoing
Refund
FoodJuly 2, 2015· Arthur Schuman Inc.

Recalled Item: Bella Rosa Parmesan Net Wt. 20 oz (567 g) 1.25 LB Arthur Schuman Recalled by...

The Issue: Bella Rosa Grated Parmesan Cheese may contain undeclared egg lysozyme.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 2, 2015· Cook Inc.

Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For...

The Issue: Reports of catheter tip splits and or separation. Loss of device function,...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2015· Cook Inc.

Recalled Item: Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in...

The Issue: Reports of catheter tip splits and or separation. Loss of device function,...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2015· Cook Inc.

Recalled Item: Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use...

The Issue: Reports of catheter tip splits and or separation. Loss of device function,...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2015· Silhouette Lift, Inc.

Recalled Item: Silhouette Lift brochure Silhouette Sutures are for use in midface Recalled...

The Issue: Silhouette Lift is recalling the Silhouette Suture brochure because it does...

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

Class II — Potential Health HazardOngoing