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.

47,654 total recalls
2,448 in last 12 months

Showing 3058130600 of 47,654 recalls

DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 21, 2016· Akorn Inc

Recalled Item: Sodium Chloride Ophthalmic Solution Recalled by Akorn Inc Due to Subpotent...

The Issue: Subpotent Drug: concentration of product is less than labeled amount.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 21, 2016· Centurion Medical Products Corporation

Recalled Item: Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The...

The Issue: The kits contain Multi-Med Single Lumen Catheters that have a potential for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...

The Issue: Recovery of Incorrect Isocenter -operational change

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens is providing software update version VA50A_SP3 to address the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...

The Issue: Software defect:2D projection of contours in Verity. The defect causes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Recalled by Merge Healthcare, Inc. Due to A product issues happens for...

The Issue: A product issues happens for RF projection images. If user measures on RF...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 20, 2016· CutisPharma, Inc.

Recalled Item: FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit Recalled by...

The Issue: Labeling: Label error on declared strength. Package Insert -Error in the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 20, 2016· CutisPharma, Inc.

Recalled Item: FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit Recalled by...

The Issue: Labeling: Label error on declared strength. Package Insert -Error in the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Cherry Raspberry Preserves 12oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Jalapeno Cherry Butter 12oz and 20oz glass bottles Recalled...

The Issue: Products contain milk not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms America's Original Cherry Butter 12oz and 22oz glass...

The Issue: Products contain milk not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Strawberry Preserves 12oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Pear & Cinnamon Preserves 10oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Michigan Cherry Preserves 12oz glass bottles and 1 Recalled...

The Issue: Products contain milk not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 19, 2016· Greatbatch Medical

Recalled Item: Offset Reamer Handle Recalled by Greatbatch Medical Due to On June 14, 2016,...

The Issue: On June 14, 2016, Greatbatch discovered a significant increase in the number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: A problem can occur with the small light marker windows, used for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CA 19-9 Assay (50 test kit)-for use Recalled by Siemens...

The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...

The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: A problem can occur with the small light marker windows, used for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing