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. 1,673 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
1,673 in last 12 months

Showing 4232142340 of 47,970 recalls

Medical DeviceOctober 23, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS brand ARTISTE Linear Accelerator Linac systems with component: any...

The Issue: A safety risk regarding a potentially existing dark current radiation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand IOLMaster Recalled by Carl Zeiss Meditec, Inc. Due to The user...

The Issue: The user database delivered for download contained an erroneous value....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS brand ONCOR series Linear Accelerator Linac systems with component:...

The Issue: A safety risk regarding a potentially existing dark current radiation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· ConMed Corporation

Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...

The Issue: The affected lots were exposed to a higher than acceptable level of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand IOLMaster 500 Recalled by Carl Zeiss Meditec, Inc. Due to The...

The Issue: The user database delivered for download contained an erroneous value....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Stryker Medical Division of Stryker Corporation

Recalled Item: Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable Recalled by...

The Issue: It was reported that the siderail may appear latched when it is not, due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· ConMed Corporation

Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...

The Issue: The affected lots were exposed to a higher than acceptable level of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Philips Medical Systems, Inc.

Recalled Item: BrightView XCT is a gamma camera for Single Photon Emission Recalled by...

The Issue: It was discovered the CT portion of the scan was interrupted ( stopping the...

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

Class II — Potential Health HazardOngoing
DrugOctober 22, 2013· Sandoz Incorporated

Recalled Item: Tacrolimus Capsules Recalled by Sandoz Incorporated Due to Cross...

The Issue: Cross Contamination with Other Products: findings of carryover of trace...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 21, 2013· Medisca Inc.

Recalled Item: Human Chorionic Gonadotropin Recalled by Medisca Inc. Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; Firm states that erroneous...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: RepairVite (K63) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: GlutenFlam (K-52) Enzyme & Bioflavonoid Dietary Supplement Recalled by Apex...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: SuperDigestZyme (Z22) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: LGS-Zyme (Z12) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 21, 2013· Applied Medical Resources Corp

Recalled Item: Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue...

The Issue: Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: THUNDER¿ Extra Support Guidewire Recalled by Medtronic Vascular Due to...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Urologix, Inc.

Recalled Item: Prostiva RF Therapy Hand Piece Kit Recalled by Urologix, Inc. Due to A Hand...

The Issue: A Hand Piece high deployment force exceeded the maximum specification.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: COUGAR¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: Zinger¿ Stainless Steel Workhorse Guidewire Recalled by Medtronic Vascular...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ Recalled by...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing