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. 2,445 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,445 in last 12 months

Showing 3318133200 of 47,654 recalls

Medical DeviceMarch 10, 2016· Repro-Med Systems, Inc.

Recalled Item: Freedom60 Precision Flow Rate Tubing Sets Recalled by Repro-Med Systems,...

The Issue: On 2/24/2016 during post sterilization inspection of part number F180...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2016· Repro-Med Systems, Inc.

Recalled Item: HIgH-Flo Subcutaneous Safety Needle Sets Recalled by Repro-Med Systems, Inc....

The Issue: On 2/24/2016 during post sterilization inspection of part number F180...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2016· Merge Healthcare, Inc.

Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to If the PDM is...

The Issue: If the PDM is utilized to output a pressure for computing fractional flow...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius 2008 Series Hemodialysis Delivery Systems: 2008T Recalled by...

The Issue: Added Warning Statement: Fresenius 2008 Series Hemodialysis Machines False...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2016· Teva Pharmaceuticals USA

Recalled Item: Amikacin Sulfate injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Presence of Particulate Matter: particulate matter identified as glass in...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 9, 2016· Whole Foods Market

Recalled Item: 365 Everyday Value Mango Frozen Fruit Bars 4 Bars-4 fl. Recalled by Whole...

The Issue: Undeclared coconut

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 9, 2016· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient...

The Issue: Panorama Central Station including the work station View Station, View...

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

Class II — Potential Health HazardOngoing
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Mannitol I.V. Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Potassium Chloride Injection 20 mEq Recalled by Hospira Inc. Due to Chemical...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Aminosyn-PF (amino acids) 7% Recalled by Hospira Inc. Due to Chemical...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 8, 2016· Hill-Rom, Inc.

Recalled Item: Liko Universal SlingBars Universal SlingBar" 350 Recalled by Hill-Rom, Inc....

The Issue: The center bolt of the sling bar, which connects the bar to the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva Emit Methotrexate Assay Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics confirmed that Syva Emit Methotrexate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing