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. 2,485 recalls have been distributed to District of Columbia in the last 12 months.
Showing 21521–21540 of 47,654 recalls
Recalled Item: Allergy Relief D Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Recalled by Sun...
The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg/ Recalled by...
The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Filter-Tips Recalled by Qiagen Sciences LLC Due to Kit lots contain a small...
The Issue: Kit lots contain a small percentage of damaged Filter-Tips that are leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PulsioFlex Monitoring System Recalled by GETINGE US SALES LLC Due to The...
The Issue: The monitor displays an error message . The error message states "internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: inLight Medical LED Pads used with Polychromatic light technology system...
The Issue: LED pads with cord connectors that have v-shaped notches may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra-Drive Irrigation Tubing Assembly Recalled by Zimmer Biomet, Inc. Due...
The Issue: The products do not have sufficient data to support the labeled shelf life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra-Drive Hose/Drape Assembly Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The products do not have sufficient data to support the labeled shelf life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The potential sporadic performance problems may cause scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The potential sporadic performance problems may cause scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The potential sporadic performance problems may cause scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The potential sporadic performance problems may cause scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol Vaginal Inserts USP 10 mcg Recalled by Glenmark Pharmaceuticals...
The Issue: Defective Delivery System: Estradiol Vaginal Inserts USP plunger is not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vereos PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due to The...
The Issue: The Vereos PET/CT may have misaligned front and rear covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion DIFFICULT IV KIT containing BD's Vacutainer Plastic Lithium...
The Issue: False elevation of carboxyhemoglobin (COHb) results in blood samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preferred Plus Dioctyl Liquid Stool Softener (Docusate Sodium) Recalled by...
The Issue: cGMP Deviations: Products may have microbial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gericare Geri-Tussin DM Recalled by Geritrex, LLC Due to cGMP Deviations:...
The Issue: cGMP Deviations: Products may have microbial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gericare Diocto Liquid Docusate Sodium Stool Softener Recalled by Geritrex,...
The Issue: cGMP Deviations: Products may have microbial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ritussin DM Children & Adults Recalled by Geritrex, LLC Due to cGMP...
The Issue: cGMP Deviations: Products may have microbial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine Oral Liquid Alcohol Free Recalled by Geritrex, LLC Due to...
The Issue: cGMP Deviations: Products may have microbial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.