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.
Showing 26981–27000 of 27,833 recalls
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: 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 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: 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: 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: 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 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: 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: 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 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: 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.
Recalled Item: Hospira LifeShield Latex-Free 100 mL Burette Set Recalled by Hospira Inc....
The Issue: The float valve in the burette sticks to the burette wall and does not open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oto Ease by Westone Recalled by Westone Laboratories, Inc. Due to Westone is...
The Issue: Westone is recalling all Oto Ease ear lubricant in all packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOMIX Plus High Speed Compounder System Recalled by Baxter Healthcare...
The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOMIX High Speed Compounder System Recalled by Baxter Healthcare Corp. Due...
The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.