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 4448144500 of 47,654 recalls

Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14217-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14211-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14212-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14210-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14203-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14206-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Roche Molecular Systems, Inc.

Recalled Item: cobas¿ 4800 system z480 instrument. Integrates fully automated total...

The Issue: In rare instances, channel shifted results have been generated with cobas¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog#...

The Issue: The firm is recalling the specific lot due to lower than expected results.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14200-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Fresenius Medical Care Holdings, Inc. dba Renal Solutions

Recalled Item: 2008 MeDS Pump Recalled by Fresenius Medical Care Holdings, Inc. dba Renal...

The Issue: Product is being recalled because the combination of the current 50 mg vial,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2013· Sysmex America, Inc.

Recalled Item: The UF-1000i is a fully automated urine particle analyzer intended Recalled...

The Issue: The current Century Break patch did not contain the same setting for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2013· Cordis Corporation

Recalled Item: Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***. No.***466F220A...

The Issue: Correction to provide clarification and additional labeling to minimize...

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

Class I — Serious Health HazardOngoing
DrugMarch 29, 2013· Hospira Inc.

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

The Issue: Presence of Particulate Matter: reports of small grey/brown particles found...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2013· Pfizer Inc.

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...

The Issue: Chemical contamination: emission of strong odor after package was opened.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2013· Pfizer Inc.

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...

The Issue: Chemical contamination: emission of strong odor after package was opened.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2013· Pfizer Inc.

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...

The Issue: Chemical contamination: emission of strong odor after package was opened..

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2013· Pfizer Inc.

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...

The Issue: Chemical contamination: emission of strong odor after package was opened

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2013· Pfizer Inc.

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...

The Issue: Chemical contamination: emission of strong odor after package was opened.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2013· Pfizer Inc.

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...

The Issue: Chemical contamination: emission of strong odor after package was opened..

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2013· Pfizer Inc.

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by Pfizer Inc. Due to...

The Issue: Chemical contamination: emission of strong odor after package was opened.

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

Class II — Potential Health HazardOngoing
Refund