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. 938 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
938 in last 12 months

Showing 37161–37180 of 47,654 recalls

DrugApril 7, 2015· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Sterility Assurance: The product has the potential to leak at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2015· Akorn, Inc.

Recalled Item: Hydroxyzine Hydrochloride Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2015· Akorn, Inc.

Recalled Item: Hydroxyzine Hydrochloride Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2015· Apotex Inc.

Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugApril 7, 2015· Apotex Inc.

Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: Assay Data Disk (ADD) Recalled by Ortho-Clinical Diagnostics Due to Software...

The Issue: Software anomaly regarding urine samples that require acidified...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly allows testing of multiple assays using a single urine...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· GA Industries

Recalled Item: Logicon Caries Detector Product Usage: Analyze inter-proximal tooth surfaces...

The Issue: GA Industries is recalling the Logicon Caries Detector, version 5.0, for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly...

The Issue: Software anomaly regarding urine samples that require acidified...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly allows testing of multiple assays using a single urine...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2015· Carefusion 211 Inc dba Carefusion

Recalled Item: CareFusion AVEA ventilator Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: A pressure transducer failure can develop, activating a false Extended High...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Elite Care Cliner w/Swing Away Arms Standard - with Recalled by Winco...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Care Cliner X-Large - with Nylon Casters Oncology Recalled by Winco...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Inverness 24-Hour Treatment Recliner - with Nylon Casters Lay Recalled...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Designer Care Cliner - with Nylon Casters Oncology Recalled by Winco...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Drop Arm Care Cliner X-Large - with Nylon Casters Oncology Recalled by...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: FLOW-i Anesthesia System The FLOW-i Anesthesia System is intended for...

The Issue: In some Flow-i Anesthesia Systems, patient cassette can get dislodged which...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Drop Arm Care Cliner Standard - with Steel Casters Oncology Recalled...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Drop Arm Care Cliner Standard - with Nylon Casters Oncology Recalled...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2015· Winco Mfg., LLC

Recalled Item: Winco Care Cliner Standart - Steel Casters Oncology Recalled by Winco Mfg.,...

The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...

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

Class II — Potential Health HazardOngoing