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. 2,373 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,373 in last 12 months

Showing 4400144020 of 47,654 recalls

DrugMay 15, 2013· Actavis South Atlantic LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution USP) 15 mg/mL Recalled by Actavis...

The Issue: Failed Impurity/Degradation Specification; "Related Compound C"

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Budesonide Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Dissolution Specifications: Routine stability testing at the 12-month...

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

Class III — Low RiskOngoing
Refund
FoodMay 15, 2013· Arthur Schuman Midwest LLC

Recalled Item: GRATED 2/25 GRANA PADANO Recalled by Arthur Schuman Midwest LLC Due to...

The Issue: Grated Grana Padano Hard Italian Cheese was tested and found to be positive...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 15, 2013· Sysmex America Inc

Recalled Item: pocH-100i Recalled by Sysmex America Inc Due to The data printed on the...

The Issue: The data printed on the thermal printer may omit a digit or decimal point in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Two Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp. Due...

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Four Lead TUR irrigation Set Recalled by Baxter Healthcare Corp. Due to A...

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Four Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp....

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Biomet, Inc.

Recalled Item: Superior Approach Resection Guide Assembly. Indicated for primary Recalled...

The Issue: Biomet has initiated this action following an investigation which identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Maytex Corp

Recalled Item: Comfort brand Ear-Loop Face Mask Recalled by Maytex Corp Due to Recent Lab...

The Issue: Recent Lab testing conducted in March 2013 indicates that the product does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· AGFA Corp.

Recalled Item: AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 Recalled by...

The Issue: Customers could potentially experience intermittent, unintended and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Edwards Lifesciences, LLC

Recalled Item: QuickDraw Venous Cannula with Insertion Kit. ThruPort Systmes. Models QD22...

The Issue: Edwards is recalling the QuickDraw Venous Cannula due to complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Optovue, Inc.

Recalled Item: Optovue iVue with Normative Database (NDB) with Software Version 3.0...

The Issue: Colors from the NDB comparison for Ganglion Cell Complex thickness in the...

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

Class III — Low RiskOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 500 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· GE Healthcare, LLC

Recalled Item: Canister: CO2 canister with GE part numbers 1407-3200-000 Recalled by GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH Calibrator 6 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur iPTH Calibrator 2 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 100 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
DrugMay 13, 2013· Abrams Royal Pharmacy

Recalled Item: Trace Mineral-5 MDV Recalled by Abrams Royal Pharmacy Due to Non-Sterility;...

The Issue: Non-Sterility; contract laboratory identified Staphylococcus warneri in the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 13, 2013· Zydus Pharmaceuticals USA Inc

Recalled Item: Warfarin Sodium Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Failed Tablet/Capsule Specifications: A product complaint was received from...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 13, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL) Recalled by...

The Issue: Failed Impurity/Degradation Specifications; out of specification value for...

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

Class III — Low RiskOngoing
Refund