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 2530125320 of 27,833 recalls

Medical DeviceJuly 1, 2013· Iradimed Corporation

Recalled Item: MRidium 1145 Dose Reduction System (DERS) drug library kit. (This Recalled...

The Issue: The Dose Error Reduction System (DERS) can indicate an incorrect recommended...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker TPS Universal Driver 99 Rx Recalled by Stryker Instruments Div. of...

The Issue: The safety margin values detailed in the Engineering Design were entered...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RemB Electric Universal Driver For use with the Recalled by Stryker...

The Issue: The safety margin values detailed in the Engineering Design were entered...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL...

The Issue: Siemens initiated a recall due to confirmed complaints of low patient sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: CORE Universal Driver 99 Rx Only This drill Recalled by Stryker Instruments...

The Issue: The safety margin values detailed in the Engineering Design were entered...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2013· Medtronic Neurosurgery

Recalled Item: Medtronic Preimplantation Test Kit Recalled by Medtronic Neurosurgery Due to...

The Issue: Medtronic Neurosurgery is recalling the Medtronic Preimplantation Test Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...

The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2013· Alphatec Spine, Inc.

Recalled Item: Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico Recalled by...

The Issue: The firm initiated this recall of certain lots of Illico Ti Cannulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Calibrator A. Cat. #04800735 Recalled by Siemens Healthcare...

The Issue: Calibrator A lot CA77 is under-recovering to the assigned target for the...

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

Class III — Low RiskOngoing
Medical DeviceJune 28, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...

The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2013· Insight Instruments, Inc.

Recalled Item: MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25-...

The Issue: The product was registered and distributed as a Class I medical device and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Healthcare Diagnostics

Recalled Item: PSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers Recalled...

The Issue: Customers complained of a positive bias in patient results on the IMMULITE/...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Mar Cor Purification

Recalled Item: Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model...

The Issue: High inlet water pressure beyond specification and the solenoid valve does...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Healthcare Diagnostics

Recalled Item: ADVIA 120 Hematology Analyzer Recalled by Siemens Healthcare Diagnostics Due...

The Issue: The ADVIA 120 optics cover or hood is located on the very top of the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS zee and zeego x-ray Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Siemens issued a customer safety advisory notice and field safety corrective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2013· Convatec Inc.

Recalled Item: ConvaTec Flexi-Seal SIGNAL + Recalled by Convatec Inc. Due to ConvaTec...

The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...

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

Class III — Low RiskOngoing
Medical DeviceJune 25, 2013· Convatec Inc.

Recalled Item: ConvaTec Flexi-Seal SIGNAL Fecal Management System Recalled by Convatec Inc....

The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...

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

Class III — Low RiskOngoing
Medical DeviceJune 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur HCY Diluent - 10mL Bottle Catalog number 09877493 (124533)...

The Issue: ADVIA Centaur Homocysteine dilution recovery on the diluent identified the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console (Console 110V with Pedal & Pole)...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-851-000(Console 100V) Product...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing