Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,360 recalls have been distributed to District of Columbia in the last 12 months.
Showing 46321–46340 of 47,654 recalls
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: 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: Dimension Vista(R) Vancomycin Flex(R) Reagent Cartridge (VANC Recalled by...
The Issue: Siemens has received complaints of customers experiencing slopes >1.05 when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RF Cannula Recalled by Stryker Instruments Div. of Stryker Corporation Due...
The Issue: Stryker has received 6 complaints that the 5mm needle was placed in 10 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RF Cannula Recalled by Stryker Instruments Div. of Stryker Corporation Due...
The Issue: Stryker has received 6 complaints that the 5mm needle was placed in 10 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-ROCK All Natural Male Supplement. 1 capsule blister pack Recalled by Coral...
The Issue: Marketed Without an Approved NDA/ANDA: Products tested positive for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: X-ROCK 3 Day Pill For Men Recalled by Coral Rock Man, Inc. Due to Marketed...
The Issue: Marketed Without an Approved NDA/ANDA: Products tested positive for...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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 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: 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: 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.