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. 1,001 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16861–16880 of 47,654 recalls
Recalled Item: Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Model...
The Issue: Potential for a false-negative result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number U1053617 - Product Usage:...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Enteric Pathogens Nucleic Acid Test (EP) Model Number: 20-006-023...
The Issue: Potential for a false-negative result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1138747 - Product...
The Issue: Ventilator may experience potential issues with the backup battery failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Gram Negative Blood Culture Nucleic Acid Test v2 (BC-GNv2) Recalled...
The Issue: Potential for a false-negative result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mesalamine Delayed-Release Tablets Recalled by AVKARE Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MassChrom Cortisol Recalled by Chromsystems Instruments & Chemicals GmbH Due...
The Issue: Control lots may not meet stability criteria and could result in increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva...
The Issue: Calibrator lots may not meet stability criteria and could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassChrom Cortisol Recalled by Chromsystems Instruments & Chemicals GmbH Due...
The Issue: Control lots may not meet stability criteria and could result in increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PryTime Medical - ER-Reboa Plus Catheter Recalled by Prytime Medical...
The Issue: There is a potential that catheters may have incorrectly marked balloon and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Art Of Tea - Feel Better tea Recalled by Art Of Tea Due to Potential...
The Issue: Firm was notified by supplier of Elder Berries of a recall due to potential...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mesalamine Delayed-Release Tablets Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Dissolution Specifications: Out-of-specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg Recalled by...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg Recalled by...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroex (chlorhexidine gluconate) Oral Rinse Recalled by Sunstar Americas,...
The Issue: Microbial Contamination of Non-sterile Products: contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G Recalled...
The Issue: The manufacturer has determined that with certain uncommon workflows there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANI Infusion Cannula 23G S - Product Usage: for use Recalled by Mani, Inc....
The Issue: Dimensions of the Luer connector parts out of specification, may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAC VU360 Recalled by GE Healthcare, LLC Due to Incorrect patient...
The Issue: Incorrect patient identification and/or patient demographic errors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANI TROCAR KIT 23G S - Product Usage: for use Recalled by Mani, Inc. -...
The Issue: Dimensions of the Luer connector parts out of specification, may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.