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. 1,788 recalls have been distributed to District of Columbia in the last 12 months.
Showing 24781–24800 of 47,654 recalls
Recalled Item: Duo-Flow IJ Full Tray Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DUO FLOW DOUBLE LUMEN CATHETER Recalled by Medical Components, Inc dba...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duo-Flow XTP Straight Full Set Recalled by Medical Components, Inc dba...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DUO FLOW CUSTOM TRAYS Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Set Recalled by Medical...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...
The Issue: Superpotent Drug: lots out of specification for elevated sodium chloride and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...
The Issue: Superpotent Drug and Failed Stability Specifications: lot out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Failed...
The Issue: Failed Stability Specifications: lot out of specification for elevated water...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...
The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diazepam Rectal Gel Recalled by Valeant Pharmaceuticals North America LLC...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Mylan...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...
The Issue: A nonsterile bulk product designated for further processing in a tray was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.