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 47301–47320 of 47,654 recalls
Recalled Item: Selectra ProS Analyzer Recalled by Vital Scientific N.V. Due to The action...
The Issue: The action was initiated due power supply failure. During a power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viva - JR Recalled by Vital Scientific N.V. Due to The action was initiated...
The Issue: The action was initiated due power supply failure. During a power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action was initiated due...
The Issue: The action was initiated due power supply failure. During a power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Selectra ProM Analyzer Recalled by Vital Scientific N.V. Due to The action...
The Issue: The action was initiated due power supply failure. During a power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viva-E Recalled by Vital Scientific N.V. Due to The action was initiated due...
The Issue: The action was initiated due power supply failure. During a power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "***Electric Systems Foot Control with Direction Only***Rx Only***" Product...
The Issue: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "***Electric Systems Foot Control****Rx Only***" Product Usage: Cutting and...
The Issue: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "***Electric Systems Foot Control with Direction and Irrigation***Rx...
The Issue: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 518 Vascular Self Expanding Stent The Zilver Vascular Stent Recalled...
The Issue: Cook Ireland received a product complaint from Japan on December 22nd, 2011....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KRD1 PedFuse Rods Recalled by SpineFrontier, Inc. Due to One of the rods in...
The Issue: One of the rods in each of two test constructs did not meet fatigue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker Orthopaedics has become aware of the potential for cracking of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Accolade Offset Rasp Handle Howmedica Osteonics...
The Issue: Stryker Orthopaedics has become aware of the potential for the above noted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineFrontier S-Lift Lock Shaft Inserter Recalled by SpineFrontier, Inc. Due...
The Issue: It has been verified through field use that there are two possible breakages...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2100 IQ Recalled by GE Healthcare, LLC Due to While...
The Issue: While performing a fluoroscopic examination on the GE Innova systems, there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare innova 3100-IQ Recalled by GE Healthcare, LLC Due to It was...
The Issue: It was discovered of a potential failure of the spectral filter mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare innova 3131-IQ Mobile X-ray system. The innova systems...
The Issue: It was discovered of a potential failure of the spectral filter mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare innova 3100 Recalled by GE Healthcare, LLC Due to It was...
The Issue: It was discovered of a potential failure of the spectral filter mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actra-SX 500 Capsules Recalled by Body Basics Inc Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA; product contains sildenafil, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Eon Mini Neurostimulation (IPG) System (Model 3788) is a 16-channel...
The Issue: As of 11/30/2011, St. Jude Medical has received 110 patient complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon (Model 3716) IPG is a dual channel Recalled by Advanced Neuromodulation...
The Issue: As of 11/30/2011, St. Jude Medical has received 110 patient complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.