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 2710127120 of 47,654 recalls

DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Q Care RX Petite Oral Cleansing & Suctioning System with Recalled by Sage...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Q.CARE Oral Cleansing & Suctioning System q4. Contains 1 Covered Yankauer...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Q.Care Oral Cleansing & Suctioning System q8. Contains 1 Covered Recalled by...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 22, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...

The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...

The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2017· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer Recalled by...

The Issue: Beckman Coulter has identified that an incorrect setting using a proprietary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Picture Archiving and Communication System (PACS) with software...

The Issue: Software update to correct several issues that include (1)Potential data...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Olympus Corporation of the Americas

Recalled Item: A20975A "Working insert Recalled by Olympus Corporation of the Americas Due...

The Issue: Olympus has received complaints about fragments of adhesive which detached...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Invivo Corporation

Recalled Item: Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive...

The Issue: Intermittent communication between the host system and the FlexCardio

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Integra LifeSciences Corp.

Recalled Item: TCC-EZ Recalled by Integra LifeSciences Corp. Due to A quarantined lot of...

The Issue: A quarantined lot of the devices was released for sale. Devices from this...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2017· Philips Electronics North America Corporation

Recalled Item: Azurion 3 M12 Recalled by Philips Electronics North America Corporation Due...

The Issue: When using the downscale option with the Allura R9 system or Azurion R1.1...

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

Class II — Potential Health HazardOngoing
DrugAugust 18, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Paroxetine tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Presence of Foreign tablets/capsules: risperidone Tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2017· Vital Rx, Inc. dba Atlantic Pharmacy and Compounding

Recalled Item: All Sterile Products within expiry Recalled by Vital Rx, Inc. dba Atlantic...

The Issue: Lack of Assurance of Sterility .

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2017· VistaPharm, Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per...

The Issue: Labeling: Not Elsewhere Classified; product is incorrectly labeled as Class...

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

Class III — Low RiskOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Bevacizumab Prefilled 30g and 31 gram 1.25mg/0.05mL Syringes Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Methylcobalamin 10mg Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Mannitol 20% Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Lidocaine Ophthalmic Gel 3.5% Recalled by Bella Pharmaceuticals, Inc. Due to...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Sodium Bicarbonate 8.4% Recalled by Bella Pharmaceuticals, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Magnesium Chloride 200mg Recalled by Bella Pharmaceuticals, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund