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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 30081–30100 of 47,654 recalls
Recalled Item: Ambrosia Quality Foods Brand 4/1 gallon Worcestershire Sauce Net 128 Fl. Oz....
The Issue: Ambrosia brand 4/1 Gallon Worcestershire Sauce may contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IMPAX Cardiovascular The IMPAX CV Reporting module consists of a Recalled by...
The Issue: A customer experienced when using IMPAX CV Reporting software, specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAKO RIO THA Application User Guides Recalled by Mako Surgical Corporation...
The Issue: Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keyspan High-High Speed USB to Serial Adapter Product Usage: The Recalled by...
The Issue: Power outages causes reporting software to shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agfa Healthcare NX 3.0.8950 Imaging Processing Software Recalled by AGFA...
The Issue: A customer reported that when using an NX workstation with software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Recalled by Siemens Healthcare Diagnostics,...
The Issue: Negative bias results with the IMMULITE¿ /IMMULITE¿ 1000 Third Generation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Recalled by Siemens Healthcare Diagnostics,...
The Issue: Negative bias with IMMULITE¿ /IMMULITE¿ 1000 Third Generation PSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Program Update Package AutoDELFIA¿ 3.0 Recalled by PerkinElmer Health...
The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELFIA¿ PC with V3.0 Software Recalled by PerkinElmer Health Sciences, Inc....
The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoDELFIA¿ Plate Processor Recalled by PerkinElmer Health Sciences, Inc....
The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008K@home Series : Hemodialysis System Recalled by Fresenius...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008K2 Series : Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T Series Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008K Series : Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Product Usage: Used to make treatment plans Recalled by...
The Issue: Incorrect Enhanced Dynamic Wedge (EDW) or Virtual Wedge (VW) Calculations.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisinopril tablets Recalled by Accord Healthcare, Inc. Due to Failed...
The Issue: Failed tablet/capsule specification: missing break line on the 5mg tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...
The Issue: Failed Dissolution Specifications; 18 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...
The Issue: Failed Dissolution Specifications; 18 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.