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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,360 in last 12 months

Showing 4676146780 of 47,654 recalls

Medical DeviceMay 25, 2012· CareFusion 303, Inc.

Recalled Item: Alaris PC unit model 8015 Product Usage: The device is Recalled by...

The Issue: The recall was initiated because the Alaris PC unit model 8015 has a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of inaccurate Scale factor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2012· GE Healthcare, LLC

Recalled Item: GE Seno Advantage 1.x Recalled by GE Healthcare, LLC Due to GE Healthcare...

The Issue: GE Healthcare has become aware of an issue associated with the magnification...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Advantage Workstations Recalled by GE Healthcare, LLC Due to...

The Issue: GE Healthcare is informing you of incorrect measurements when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2012· GE Healthcare, LLC

Recalled Item: GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume...

The Issue: GE Healthcare has become aware of a potential safety issue due to incorrect...

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

Class II — Potential Health HazardOngoing
FoodMay 23, 2012· Mitsui Foods Inc

Recalled Item: Whole Oysters: 1) Empress Whole Oysters Recalled by Mitsui Foods Inc Due to...

The Issue: As of May 1, Korean shellfish imports have been blocked by the United States...

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

Class III — Low RiskOngoing
Refund
FoodMay 23, 2012· Mitsui Foods Inc

Recalled Item: Smoked Oysters: 1) Empress Smoked Oysters In Cottonseed Oil Recalled by...

The Issue: As of May 1, Korean shellfish imports have been blocked by the United States...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 23, 2012· LMA North America Inc

Recalled Item: LMA Esophageal Intubation Detector (EID) Recalled by LMA North America Inc...

The Issue: The recall was initiated because LMANA has received a complaint that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2012· Integra Limited

Recalled Item: Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R)...

The Issue: The Integra(TM) Jarit(R) Take-Apart Laparoscopic Instrument shafts were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2012· Stingray Surgical Products, LLC

Recalled Item: Bipolar Forceps model number: S02-XXX Recalled by Stingray Surgical...

The Issue: On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton, FL initiated a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: IntelliSpace Portal software and Extended Brillance Workspace software...

The Issue: The Intellispace Portal software and Extended Brillance Workspace software...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Intellispace Portal software. Intellispace Portal is a multimodality thin...

The Issue: Philips is issuing a software update to the Intellispace Portal systems to...

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

Class II — Potential Health HazardOngoing
FoodMay 22, 2012· World Finer Foods, Inc.

Recalled Item: Da Vinci Pesto Genovese with basil and pine nuts Net Recalled by World Finer...

The Issue: Da Vinci Pesto Genovese with Basil and Pine Nuts 10 oz. is mislabeled as the...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 22, 2012· Indonesian Food Mart

Recalled Item: Tempeh Starter Yeast Recalled by Indonesian Food Mart Due to Potential...

The Issue: Imported food product tested positive for Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 22, 2012· Indonesian Food Mart

Recalled Item: Tempeh Super Starter Yeast Recalled by Indonesian Food Mart Due to Potential...

The Issue: Imported food product tested positive for Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 22, 2012· Beckman Coulter Inc.

Recalled Item: CYTO-STAT tetraCHROME CD45-FITC/CD4-RD1/CD8-ECD/CD3-PC5 Recalled by Beckman...

The Issue: The recall was initiated because Beckman Coulter has determined that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Beckman Coulter Inc.

Recalled Item: TetraCXP Software System Recalled by Beckman Coulter Inc. Due to The recall...

The Issue: The recall was initiated because Beckman Coulter has determined that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Beckman Coulter Inc.

Recalled Item: CYTO-STAT tetraCHROME CD45- FITC/CD56-RD1/CD19-ECD/CD3-PC5 Recalled by...

The Issue: The recall was initiated because Beckman Coulter has determined that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Becton Dickinson & Co.

Recalled Item: BD GeneOhm MRSA ACP Assay Catalog #441637 Recalled by Becton Dickinson & Co....

The Issue: Leakage in Cepheid SmartCycler reaction tubes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Becton Dickinson & Co.

Recalled Item: BD GeneOhm VanR Assay Recalled by Becton Dickinson & Co. Due to Leakage in...

The Issue: Leakage in Cepheid SmartCycler reaction tubes.

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

Class II — Potential Health HazardOngoing