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. 2,622 recalls have been distributed to District of Columbia in the last 12 months.
Showing 6561–6580 of 27,451 recalls
Recalled Item: VersaOne Reusable Positioning Cannula 8 mm Standard Recalled by Covidien LP...
The Issue: There is a manufacturing non-conformance that may result in a metal shaving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software Recalled by...
The Issue: Upon installation of BD Kiestra" InoqulA+" and BeA version 5.1 and 5.1.1 as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion System with software versions: R2.2.O Recalled by PHILIPS...
The Issue: Potential Loss of X-ray-When the full disk capacity is reached, X-Ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and...
The Issue: Potential for the spring to become loose and fall out of the device, if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS one with a hybrid cable- An angiography system developed Recalled by...
The Issue: Examination room monitor connected with the hybrid cable may have a display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813...
The Issue: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814...
The Issue: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DERMLITE DL4W Recalled by DermLite LLC Due to Incorrect labeling; Package...
The Issue: Incorrect labeling; Package labeling contains a different serial number then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500 Computed Tomography X-Ray System Recalled by Philips North...
The Issue: Pressing the Unload Pedal of the foot switch to perform the unload function...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...
The Issue: Light handle covers may separate from the light handle (detach and fall off)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...
The Issue: Light handle covers may separate from the light handle (detach and fall off)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery....
The Issue: Device suddenly and forcefully disassembled after cryotherapy, potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SenSight Extension Tunneler Kit Recalled by Medtronic...
The Issue: Medtronic has received reports of SenSight Extension Tunneler kits that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integre Pro Yellow LP561 Recalled by Ellex Medical Pty Ltd. Due to When...
The Issue: When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Cortisol 50T (Material Number 10995538) Recalled by Siemens...
The Issue: There is a negative bias with urine patient samples and urine cortisol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Cortisol 50T (Material Number 10994924) Recalled by Siemens...
The Issue: There is a negative bias with urine patient samples and urine cortisol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JULIET Ti LL Recalled by SPINEART SA Due to JULIET Lateral Lumbar Ti-Life...
The Issue: JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Access Free T3 Recalled by Beckman Coulter, Inc. Due to The...
The Issue: The reagent lot produces elevated results (approximately >30%) in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF) Recalled by...
The Issue: Potential shearing of the disposable blade may occur and be contained within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-C6 Recalled by Hamilton Medical AG Due to Software error causes,...
The Issue: Software error causes, safety ventilation, in which ventilation continues in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.