Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,395 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,395 in last 12 months

Showing 2660126620 of 27,833 recalls

Medical DeviceOctober 19, 2012· American Medical Systems, Inc.

Recalled Item: AMS AdVance" Male Sling System 720088-01 AMS AdVance" Male Sling Recalled by...

The Issue: American Medical Systems¿ (AMS) is issuing a voluntary recall on a number of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· Innovative Magnetic Resonance Imaging Systems Inc.

Recalled Item: IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00)...

The Issue: IMRIS Inc. initiated a recall of their OR Tables ORT100 and ORT200. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· Trivascular, Inc

Recalled Item: TriVascular brand Fill Polymer Kit Recalled by Trivascular, Inc Due to...

The Issue: Selected lots of the Fill Polymer Kit (European Model Number: TVFP14- B) in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2012· OrthoPediatrics Corp

Recalled Item: 4.5mm PLEO Osteotomy Guide. OrthoPediatrics Corp. markets a pediatric...

The Issue: Complaint received from sales representative that the drill guide tubes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2012· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Multi-Sliced CT Scanner System Recalled by Philips And Neusoft...

The Issue: The four screws that secure the patient table top to the carrier pulled out...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2012· Biomerieux Inc

Recalled Item: 0.9% Sodium Chloride Injections Recalled by Biomerieux Inc Due to The firm...

The Issue: The firm inventoried and distributed 0.9% Sodium Chloride Saline bags as...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Tested AC Control BD Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: HX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management Recalled by...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Vital Signs Devices, a GE Healthcare Company

Recalled Item: Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal...

The Issue: Thirty fetal scalp electrodes were found to have an incomplete package seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· Ossur Americas, Inc.

Recalled Item: The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral Recalled...

The Issue: OSSUR is recalling the Symbionic Leg because it is not recognizing the low...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· Toshiba American Medical Systems Inc

Recalled Item: MRT-1504/A4 - Titan X MRI System MRT-30 I0A/5 - Titan Recalled by Toshiba...

The Issue: It was found that there is a problem with the LCD monitor used in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· Invivo Corporation

Recalled Item: Invivo Corporation Expression MRI Patient Monitoring System. The Expression...

The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare - Giraffe and Panda T-Piece Resuscitation System The Recalled...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 15, 2012· GE Healthcare, LLC

Recalled Item: Giraffe and Panda Bag and Mask Resuscitation System The T-piece Recalled by...

The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 12, 2012· MOOG Medical Devices Group

Recalled Item: Infinity Enteralite Ambulatory Feeding Pumps Recalled by MOOG Medical...

The Issue: The firm is adding an addendum to the operator's manual for Infinity...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Liberty Cycler Set Single Conn. Ext. DL. Part Number: Recalled by...

The Issue: There is a small risk of a leak in Cycler Sets and if the Cycler Set is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2012· GE Healthcare, LLC

Recalled Item: GE Discovery NM/CT670 Recalled by GE Healthcare, LLC Due to GE Healthcare...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens StreamLAB(R) Analytical Workcell Recalled by Siemens Healthcare...

The Issue: Firm has received reports from customers that the small pins at the bottom...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: The Stryker Model 6390 Recalled by Stryker Medical Division of Stryker...

The Issue: Model 6390 Power-LOAD systems built between September 12, 2012 and September...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mobilette Mira Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: There is a risk of lost images during examination.

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

Class II — Potential Health HazardOngoing