Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,363 recalls have been distributed to North Dakota in the last 12 months.
Showing 26661–26680 of 27,512 recalls
Recalled Item: Dimension(R) Reagent Management System (RMS) - Power Cord. The Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed that partial insertion of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Syphilis (SYPH) Assay Recalled by Siemens Healthcare...
The Issue: Syphilis Assay Interference with HBsAg Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conformis iTotal CR-Cruciate Retaining Knee Replacement System Model...
The Issue: Addendum Labeling iTotal CR Surgical Technique with Detailed Instructions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: djo surgical Screw 6.5 mm Recalled by Encore Medical, Lp Due to Mislabeling
The Issue: One lot of the 010-55-030, 6.5 mm Cancellous Bone Screw was recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IR1200 Recalled by Animas Corporation Due to Wear of the keypad that may...
The Issue: Wear of the keypad that may lead to damage such as tearing or peeling of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightCycler 2.0 Instrument (software version 4.1) is a Rapid PCR Recalled by...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DataCare POC is an information management system that provides Recalled by...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MagNA Pure 96 System (versions 1.0 and 2.0) is Recalled by Roche...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightCycler 1.2 (software version 3.5) is a Rapid PCR analyzer Recalled by...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MagNA Pure LC (version 3.0) is a sample preparation Recalled by Roche...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The COBAS 8000 data manager modular analyzer series (all versions) Recalled...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DataInnovations (Instrument Manager) (version 8.04) interfaces middleware...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Data Station AMPLILINK software is an instrument user interface/ data...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The COBAS INTEGRA 400/400 plus system (software version 3.4) is Recalled by...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DataCara GM is an information management system that provides data Recalled...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Special Orthopaedic Solution Peri-Acetabular Prosthesis V40 Femoral...
The Issue: Stryker has become aware that insufficient taper torsional strength may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enduramesh Corpectomy Spacer System Product Usage: The Enduramesh is a...
The Issue: The firm voluntarily recalled the device after they discovered that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Electroblade Resector Recalled by Smith & Nephew,...
The Issue: Devices labeled with an expiry period of 48 months instead of 36 months; an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Reliance 130 and 130L Cart Washer/Disinfector is a high Recalled by...
The Issue: To ensure that users are properly operating the Reliance 130 and 130L Cart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm Dyonics Bonecutter Recalled by Smith & Nephew, Inc....
The Issue: Device labeled with an expiry period of 48 months instead of 36 months; an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.