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. 2,438 recalls have been distributed to District of Columbia in the last 12 months.
Showing 34921–34940 of 47,654 recalls
Recalled Item: Philips X-Ray Systems Recalled by Philips Electronics North America...
The Issue: Upon initiating Fluoroscopy the user may encounter a user message Fluoro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burn Relief¿ Recalled by O-Two Medical Technologies, Inc. Due to For lack of...
The Issue: For lack of evidence to validate effectiveness of sterilization dose, O-Two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rhino 7 3000 Recalled by Premiere Sales Group Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 Platinum 3000 Recalled by Premiere Sales Group Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension Vista System (MG) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Erroneous low results on a small number of reagent wells. There is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD CD3 (SK7) FITC Recalled by Becton, Dickinson and Company, BD Biosciences...
The Issue: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.
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 is recalling various lots of the Trithion MIS Modular Distal Capture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Achieve Cables Recalled by Medtronic Inc. Due to 64 units of...
The Issue: 64 units of Achieve Electrical Cables were shipped with a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amidate (Etomidate Injection Recalled by Hospira Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification(OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultimate Herbal Slimcap Capsules Recalled by Fit Firm and Fabulous Due to...
The Issue: Marketed Without An Approved NDA/ANDA: product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine HCl 10 mg Tablet Recalled by Perrigo Company PLC Due to Failed...
The Issue: Failed Impurity/Degradations Specifications; impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 9 Calibrator Recalled by...
The Issue: The firm is conducting a product correction due to an increase in U90-382 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Universal Viewer Version is a device that displays Recalled...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Due to An...
The Issue: An anomaly was identified with the ARIA for Radiation Oncology software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS-IW with Universal Viewer is a device that Recalled by GE...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Radius 5.5 to 3.5 Rod to Red Connector Recalled by Stryker Spine Due...
The Issue: Stryker Spine is recalling Radius Rod to Rod Connector 5.5 to 3.5 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACETAMINOPHEN EXTRA-STRENGTH PAIN RELIEVER tablets Recalled by Medline...
The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 Platinum 3000 Recalled by Tf Supplements Due to Undeclared Desmethyl
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RHINO 7 3000 Recalled by Tf Supplements Due to Undeclared Desmethyl
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets Recalled by Medline...
The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.