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. 2,464 recalls have been distributed to District of Columbia in the last 12 months.
Showing 22801–22820 of 27,451 recalls
Recalled Item: Codman EDS 3 Drainage System with Ventricular Catheter (External Drainage...
The Issue: tubing within the system that drains CSF may leak or disconnect from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Systems HBc Total (HBcT) Recalled by Siemens...
The Issue: Increased imprecision and positive bias is observed with patient samples and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿¿ Systems HBc Total (HBcT) Kit. For In Vitro Recalled by...
The Issue: Increased imprecision and positive bias is observed with patient samples and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Expression Information Portal (IP5) Model 865471. The IP5 is...
The Issue: Frozen Display Numerics and Disabled Menu Keys after extended run time. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer. The Roche...
The Issue: The default for normal values are inconsistent between cobas b 221 and other...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ and ADVIA Centaur¿ XP and ADVIA Centaur¿ CP Recalled by...
The Issue: Stability of the ADVIA Centaur Cleaning Solution is not assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prescription eyeglass safety lenses. Vision correction Recalled by Eyemart...
The Issue: Prescription eyeglass safety lenses did not meet specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSEMBLY Recalled by Intuitive Surgical, Inc. Due to Correction due to the...
The Issue: Correction due to the detection of a motor sensor failure in the Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 Recalled by Abbott...
The Issue: 17% of ARCHITECT Total T3 Reagent Kit, LN 7K64-20/-25 reagent lots 38901UI00...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona The Personalized Knee System 2.5 mm Female Screw 48 Recalled by...
The Issue: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: An endometrial suction curette is a device used to remove Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lock nuts for titanium traction tongs are used in traction Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson braces are bone cutting and drilling instruments that are Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement screw non-springloaded traction tongs are skull tongs for...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Traction tong replacement screws Recalled by Instrumed International, Inc....
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson cerebellar extensions are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual trephines are bone cutting and drilling instruments that are Recalled...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cushing burrs are bone cutting and drilling instruments that are Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tonometers are manual devices intended to measure intraocular pressure by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: An external vein stripper is an extravascular device used to Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.